K201162 · Shenyang Torch-Bigtide Digital Technology Co., Ltd. · DXJ · Aug 27, 2020 · Cardiovascular
Device Facts
Record ID
K201162
Device Name
Essence 55SP Large Monitor System
Applicant
Shenyang Torch-Bigtide Digital Technology Co., Ltd.
Product Code
DXJ · Cardiovascular
Decision Date
Aug 27, 2020
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 870.2450
Device Class
Class 2
Indications for Use
The Essence 55SP Large Monitor System (Essence 55SP) is intended to be used by health care professionals to integrate the video output from various commercially-available instruments commonly used in a medical procedure laboratory into a single video display.
Device Story
The Essence 55SP is a 55-inch TFT color LCD monitor designed for medical procedure laboratories. It functions as a large-format display to integrate and rearrange video feeds from multiple medical instruments. Inputs are received via DVI or DisplayPort, optionally processed through a video wall controller (AVS-540) or optical graphic extension module. The device is operated by healthcare professionals to view clinical images on a single screen, facilitating situational awareness during procedures. The system includes an additional protective glass layer compared to its predicate. It provides high-resolution visualization (3840 x 2160) to assist clinicians in monitoring patient data and procedural progress, potentially improving workflow efficiency in the lab.
Clinical Evidence
Bench testing only. No clinical or animal data provided. Validation included display bench tests, display validation tests, and system tests confirming performance characteristics are equivalent to the predicate.
Technological Characteristics
55-inch TFT color LCD panel with In-Plane Switching (IPS) technology. Native resolution 3840 x 2160; 1.07 billion colors; 1400:1 contrast ratio. Inputs: DVI-D, DisplayPort, DVI single link (HDMI). Power: 100-240 VAC. VESA 400x400 mounting. IP20 protection. Backlight sensors for calibration. Complies with IEC 60601-1, ANSI/AAMI ES60601-1, and DIN V 6868-57 for brightness uniformity.
Indications for Use
Indicated for use by healthcare professionals in medical procedure laboratories to integrate video output from various commercially-available instruments into a single display.
Regulatory Classification
Identification
A medical cathode-ray tube display is a device designed primarily to display selected biological signals. This device often incorporates special display features unique to a specific biological signal.
{0}------------------------------------------------
Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: a symbol on the left and the FDA name and title on the right. The symbol on the left is a stylized representation of a human figure, while the text on the right reads "FDA U.S. FOOD & DRUG ADMINISTRATION" in blue letters.
August 27, 2020
Shenyang Torch-Bigtide Digital Technology Co., Ltd. Fu Ailing Document Engineer No. 18-6B, Yaoyang Road, Huishan Economic Development Area, Shenbei New District Shenyang, Liaoning 110164 China
Re: K201162
Trade/Device Name: Essence 55SP Large Monitor System Regulation Number: 21 CFR 870.2450 Regulation Name: Medical Cathode-Ray Tube Display Regulatory Class: Class II Product Code: DXJ Dated: July 22, 2020 Received: July 29, 2020
Dear Ms. Fu Ailing:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's
{1}------------------------------------------------
requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
for
Jennifer Shih Assistant Director DHT2A: Division of Cardiac Electrophysiology, Diagnostics and Monitoring Devices OHT2: Office of Cardiovascular Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
{2}------------------------------------------------
#### Indications for Use
510(k) Number (if known) K201162
Device Name Essence 55SP Large Monitor System
Indications for Use (Describe)
The Essence 55SP Large Monitor System (Essence 55SP) is intended to be used by health care professionals to integrate the video output from various commercially-available instruments commonly used in a medical procedure laboratory into a single video display.
Type of Use (Select one or both, as applicable):
| <span style="font-size:100%;">☒</span> Prescription Use (Part 21 CFR 801 Subpart D) | <span style="font-size:100%;">☐</span> Over-The-Counter Use (21 CFR 801 Subpart C) |
|-------------------------------------------------------------------------------------|------------------------------------------------------------------------------------|
|-------------------------------------------------------------------------------------|------------------------------------------------------------------------------------|
#### CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
#### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
> Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
{3}------------------------------------------------
# 007_510 (k) Summary
{4}------------------------------------------------
# 510(k) Summary
[As required by 21 CFR 807.92]
## 1. Date Prepared [21 CFR807.92 (a) (1)]
April 15, 2020
# 2. Submitter's Information [21 CFR807.92 (a) (1)]
| Name of Sponsor: | Shenyang Torch-Bigtide Digital Technology Co., Ltd. |
|------------------|-------------------------------------------------------------------------------------------------------------|
| Address: | No. 18-6B, Yaoyang Road, Huishan Economic Development Area,<br>Shenbei New District, 110164 Shenyang, China |
| Contact Name: | Fu Ailing |
| Telephone No.: | +86-24-88087606 |
| Fax No.: | +86-24-88087629 |
| Email Address: | btfda@bigtide.com |
### 3. Trade Name, Common Name, Classification [21 CFR807.92 (a) (2)]
| Trade Name/Model: | Essence 55SP Large Monitor System (Essence 55SP |
|-----------------------|-------------------------------------------------|
| Common Name: | Essence 55SP Large Monitor System |
| Classification Name: | Display, Cathode-Ray, Tube, Medical |
| Regulation Number: | 21 CFR 870.2450 |
| Product code: | DXJ |
| Classification Panel: | Cardiovascular |
| Device Class: | II |
# 4. Identification of Predicate Device(s) [21 CFR 807.92(a) (3)]
The identified predicate within this submission is as follow:
Shenyang Torch-Bigtide Digital Technology Co., Ltd., Essence 55S Large Monitor System has been cleared by FDA through 510(k) No. K172969 (Decision Date - February 6, 2018).
{5}------------------------------------------------
# 5. Description of the Device [21 CFR 807.92(a) (4)]
The system consists of the following components:
- A 55" TFT color LCD Monitor: HL5501SP ●
- Video wall controller (AVS-540) (optional) ●
- Optical graphic extension module-fibres detachable (M1-201SA-TR) (optional) ●
- . A common PC (optional)
- Cables (optional) .
The Essence 55SP Large Monitor System is a large color LCD monitor for viewing images derived from several video sources on a single display and to rearrange these images to the situational requirements of the user. Thanks to the advantages of the large widescreen monitor, the data can be collected from the video sources using the optional video wall controller AVS-540 and fed into the large display via the DVI lines and / or DP. DVI lines mean the assemblies consisting of DVI cable and related connectors; DP means the assembly consisting of DP cable and related connectors.
The optical graphic extension module M1-201SA-TR can be used to convert / transmit the video signal, and the common PC can be taken as a video device.
The difference between the Essence 55SP and the legally marketed device Essence 55S is additional glass. Essence 55S is without glass and Essence 55SP with glass, so Essence 55SP is named with the letter "P".
## 6. Intended Use [21 CFR 807.92(a)(5)]
- Indications for Use:
The Essence 55SP Large Monitor System (Essence 55SP) is intended to be used by health care professionals to integrate the video output from various commercially -available instruments commonly used in a medical procedure laboratory into a single video display.
### 7. Technological Characteristics [21 CFR 807.92(a)(6)]
The Essence 55SP Large Monitor System (Essence 55SP) uses a color LCD panel employing In-Plane Switching (IPS) technology to allow wide viewing angles. It is used in landscape mode.
{6}------------------------------------------------
When the various video sources from medical and other devices are being collected, they are being fed into the large Display via the corresponding lines and / or DP. The optional optical graphic extension module can be used as an optional part of the system to convert / transmit the video signal, and the optional PC can be taken as a video device.
The Essence 55SP Large Monitor System (Essence 55SP) may be provided in different housing colors and with different logos. The cosmetic differences do not affect the function and performance of the system.
| Panel Type | TFT Color LCD Panel (IPS) |
|----------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Panel Size | 139.7 cm / 55"<br>(1, 397 mm diagonal) |
| Display Size (H x V) | 1209.6 mm x 680.4 mm |
| Pixel Pitch | 0.315 x 0.315 mm |
| Native Resolution | 3840 x 2160 pixels |
| Display Colors | 1.07 billion colors |
| Viewing Angle (H,V) | 178°, 178° |
| Brightness (Typ.) | 540 cd/m² |
| Recommended Brightness for Calibration | 400 cd/m² |
| Brightness Uniformity | DIN V 6868-57 |
| Contrast Ratio (Typ.) | 1400:1 |
| Response Time (Typ.) | 18 ms |
| Scanning Frequency (H, V) | 131.3 KHz, 59.5 – 60.5 Hz |
| Dot Clock | 277 MHz |
| Input Terminals | DVI-D (dual link) x 2;<br>DisplayPort x 2;<br>DVI single link (HDMI) x 2 |
| Power Requirements | 100-240 VAC, 50/60 Hz, 3.2 - 1.2A |
| Power Consumption / Save Mode | 300 W / Less than 40 W |
| Power Management | DVI DMPM |
| Sensor | Backlight<br>Sensor x 3 |
| | |
| Net Weight | 49.5 +/- 2 Kg |
| Hole Spacing | VESA standard<br>400 x 400 mm |
| Degree of Protection | IP20 |
| Operating Temperature | 5℃ - 40℃ |
| Storage Temperature | -20℃ - 70℃ |
| Operating Humidity | 20% to 80% rel. H., non condensing |
| Storage Humidity | 10% to 95% rel. H., non condensing |
| Operating Pressure | 700 hPa - 1060 hPa |
| Storage Pressure | 700 hPa - 1060 hPa |
| Certifications and Standards* | CE: 93/42/EEC: Medical Device<br>Directive<br>Test Report CE Declaration<br>CCC Certificate<br>BIS Certificate - INDIA<br>CB-Test Certificate: IEC<br>60601-1:2005 + A1:2012 (Ed. 3.1)<br>CB-Test Report: IEC 60601-1:2005<br>+ A1:2012 (Ed. 3.1)<br>NRTL Certificate (US/C):<br>ANSI/AAMI<br>ES60601-1:2005/(R2012) +<br>CAN/CSA C22.2-60601-1-14 |
| Supplied Accessories | AC power cord |
| Optional accessories | Video wall controller (AVS-540)Optical graphic extension module-fibres detachable (M1-201SA-TR)A common PCCablesCD (user's manual) |
| Warranty | Three years |
| Order No. | HL5501SP |
| Dimmensions (Unit:mm) | 1287.2 x 761.2 x 86.3 mm |
{7}------------------------------------------------
{8}------------------------------------------------
# 8. Substantial Equivalence [21 CFR 807.92(b) (1) and 807.92]
#### 8.1 Intended uses:
| ID | Comparison<br>Item | Proposed Device<br>Essence 55SP Large Monitor<br>System | Predicate Device<br>Essence 55S Large Monitor<br>System |
|----|------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| 1 | Indications<br>for Use | The Essence 55SP Large<br>Monitor System (Essence 55SP)<br>is intended to be used by health<br>care professionals to integrate<br>the video output from various<br>commercially-available<br>instruments commonly used in a<br>medical procedure laboratory<br>into a single video display. | The Essence 55S Large<br>Monitor System (Essence 55S)<br>is intended to be used by health<br>care professionals to integrate<br>the video output from various<br>commercially-available<br>instruments commonly used in<br>a medical procedure laboratory<br>into a single video display. |
#### Table 1 Intended Use Comparison
#### 8.2 Comparison table
| | Table 2 General Comparison |
|--|-----------------------------|
| | |
| ID | Comparison<br>Item | Proposed Device<br>Essence 55SP<br>Large Monitor<br>System | Predicate Device<br>Essence 55S<br>Large Monitor<br>System | Explanation<br>of<br>Difference |
|------|----------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------|
| 2 | Display Performance/Specifications | | | |
| 2.1 | Cabinet Color | Black Grey | Black Grey | - |
| 2.2 | Panel Type | TFT Color LCD<br>Panel (IPS) | TFT Color LCD<br>Panel (IPS) | - |
| 2.3 | Panel Size | 139.7 cm / 55"<br>(1, 397 mm<br>diagonal) | 139.7 cm / 55"<br>(1, 397 mm<br>diagonal) | - |
| 2.4 | Display Size (H x<br>V) | 1209.6 mm x 680.4<br>mm | 1209.6 mm x 680.4<br>mm | - |
| 2.5 | Pixel Pitch | 0.315 x 0.315 mm | 0.315 x 0.315 mm | - |
| | | | | |
| 2.6 | Native Resolution | 3840 x 2160 pixels | 3840 x 2160 pixels | - |
| 2.7 | Display Colors | 1.07 billion colors | 1.07 billion colors | - |
| 2.8 | Viewing Angle<br>(H,V) | 178°, 178° | 178°, 178° | - |
| 2.9 | Brightness (Typ.) | 540 cd/m² | 560 cd/m² | The same<br>screen is<br>used, but<br>55SP is with<br>additional<br>glass. |
| 2.10 | Recommended<br>Brightness for<br>Calibration | 400 cd/m² | 400 cd/m² | - |
| 2.11 | Brightness<br>Uniformity | DIN V 6868-57 | DIN V 6868-57 | - |
| 2.12 | Contrast Ratio<br>(Typ.) | 1400:1 | 1400:1 | - |
| 2.13 | Response Time | 6.5 ms (Midtone) | 6.5 ms (Midtone) | - |
| 3 | Video Signal Input | | | |
| 3.1 | Scanning<br>Frequency (H, V) | 131.3 KHz, 59.5 –<br>60.5 Hz | 131.3 KHz, 59.5 –<br>60.5 Hz | - |
| 3.2 | Dot Clock | 277 MHz | 257.4 MHz | EDID is<br>changed,<br>which does<br>not raise any<br>new issue of<br>substantial<br>equivalence. |
| 3.3 | Input Terminals | DVI-D (dual link) x 2;<br>DisplayPort x 2;<br>DVI single link<br>(HDMI) x 2 | DVI-D (dual link) x 2;<br>DisplayPort x 2;<br>DVI single link<br>(HDMI) x 2 | - |
| 4 | | Power Related Specifications | | |
| 4.1 | Power<br>Requirements | AC 100-240 V, 50 /<br>60Hz, 3.2 - 1.2A | AC 100-240 V, 50 /<br>60Hz, 3.2 - 1.2A | - |
| 4.2 | Power<br>Consumption /<br>Save Mode | 300 W / Less than 40<br>W | 300 W / Less than 40<br>W | - |
| 4.3 | Power<br>Management | DVI DMPM | DVI DMPM | - |
| 5 | Miscellaneous Features/Specifications | | | |
| 5.1 | Sensor | Backlight<br>Sensor x 3 | Backlight<br>Sensor x 3 | - |
| 5.2 | Net Weight | $49.5 + /- 2 Kg$ | $38 + /- 1 Kg$ | The 55SP is with additional glass. |
| 5.3 | Hole Spacing | VESA standard<br>400 x 400 mm | VESA standard<br>400 x 400 mm | - |
| 5.4 | Supplied<br>Accessories | AC power cord, CD<br>(user' manual) | AC power cord, CD<br>(user' manual) | - |
| 5.5 | Optional<br>accessories | Video wall controller<br>(AVS-540),<br>Optical graphic<br>extension<br>module-fibres<br>detachable<br>(M1-201SA-TR),<br>a common PC,<br>Cables | Video wall controller<br>(AVS-540),<br>Optical graphic<br>extension<br>module-fibres<br>detachable<br>(M1-201SA-TR),<br>a common PC,<br>Cables | - |
| 5.6 | Order No. | HL5501SP | HL5501S | Different coding rule |
| 5.7 | Dimmensions<br>(Unit:mm) | 1287.2 x 761.2 x<br>86.3 mm | 1287.2 x 761 x 85.6<br>mm | The 55SP is with additional glass. |
{9}------------------------------------------------
{10}------------------------------------------------
It is clear that the technological characteristics differences discussed above do not affect the safety and the effectiveness of the Essence 55SP.
#### 8.3 Performance Testing
The following tests were successfully performed to validate the Essence 55SP Large Monitor System.
- Display bench tests ●
- . Display validation tests
- . System tests
The test results showed that the Essence 55SP Large Monitor System is with display characteristics equivalent to those of the predicate device, Essence 55S Large Monitor System except some items, each of which was determined that it would not affect observer's performance.
No animal or clinical testing is needed for the Essence 55SP.
{11}------------------------------------------------
## 9. Conclusion [21 CFR 807.92(b) (3)]
In accordance with the Federal Food, Drug and Cosmetic Act, 21 CFR Part 807 and based
on the information provided in this premarket notification. Shenyang Torch-Bigtide Digital
Technology Co., Ltd. concludes that:
- The intended use of Essence 55SP Large Monitor System (Essence 55SP) is totally . same as that of the predicate device.
- . The technological characteristics differences between 55SP Large Monitor System and 55S Large Monitor System do not raise different questions of safety and effectiveness.
- . Demonstrated by the bench tests, the display characteristics of Essence 55SP Large Monitor System are substantially equivalent to those of the predicate device.
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.