K071181 · Konica Minolta Medical & Graphic, Inc. · MQB · May 30, 2007 · Radiology
Device Facts
Record ID
K071181
Device Name
DIRECT DIGITIZER, REGIUS MODEL 110
Applicant
Konica Minolta Medical & Graphic, Inc.
Product Code
MQB · Radiology
Decision Date
May 30, 2007
Decision
SESE
Submission Type
Special
Regulation
21 CFR 892.1680
Device Class
Class 2
Indications for Use
The Direct Digitizer, REGIUS Model 110 is an X-ray image reader which uses a stimulable phosphor plate (Plate) as X-ray detector installed in a separate cassette. It reads the image recorded on the Plate and transfers the image data to an externally connected device such as a host computer, an order input device, an image display device, a printer, an image data filing device, and other image reproduction devices. REGIUS Model 110 also reads the image data of long areas of anatomy and to verify the position for a radiotherapy location. It is designed and intended to be used by trained medical personnel in a clinic, a radiology department in a hospital and in other medical facilities. This device is not Intended for use with digital mammography system.
Device Story
Direct Digitizer REGIUS Model 110 is a computed radiography (CR) image reader. Input: latent X-ray images recorded on stimulable phosphor plates within cassettes. Operation: laser scanning and photoelectric conversion of latent images into digital data. Output: digital image data transferred to external systems (host computers, displays, printers, filing devices). Usage: clinical/hospital radiology departments by trained personnel. Compact design modification of predicate; utilizes same technology as REGIUS Model 190 and 150. Supports long-anatomy imaging and radiotherapy positioning verification. Benefits: enables digital conversion of radiographic images for diagnostic and therapeutic planning.
Clinical Evidence
No clinical data provided. Substantial equivalence is based on bench testing and comparison of technological characteristics to the predicate device.
Technological Characteristics
Computed radiography reader using stimulable phosphor plates. Laser scanning and photoelectric detection. Compact form factor. Connectivity: digital data transfer to external workstations/printers. Compliance: IEC60601-1, IEC60601-1-2, 21 CFR 1040.10, IEC60825-1.
Indications for Use
Indicated for trained medical personnel in clinics, hospitals, and medical facilities to read X-ray images from stimulable phosphor plates for general radiographic imaging and radiotherapy positioning. Not for use with digital mammography systems.
Regulatory Classification
Identification
A stationary x-ray system is a permanently installed diagnostic system intended to generate and control x-rays for examination of various anatomical regions. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
Special Controls
*Classification.* Class II (special controls). A radiographic contrast tray or radiology diagnostic kit intended for use with a stationary x-ray system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.
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# 510(k) Summary
K071181
#### As required by 807.92
MAY 3 0 2007
## 1. Company Identification
Konica Minolta Medical & Graphic, Inc. 2970 Ishikawa-machi, Hachioji-shi, Tokyo 192-8505, Japan Phone: 81-42-660-9607 Fax: 81-42-660-9588
### 2. Official Correspondent Koji Matsushima (Mr.) Manager
Standards & Regulations Department, Quality Assurance Center
# 3. Date of Submission
April 26, 2007
## 4. Establishment Registration No. 3003769120
## 5. Device Trade Name Direct Digitizer, REGIUS Model 110
#### 6. Common Name
Computed Radiography Image Reader
#### 7. Classification
Class II, 90 MQB, 21 CFR 892. 1630.
#### 8. Predicate Device
Direct Digitizer, REGIUS Model 190, 510(k) number: K052095
#### 9. Description of Device
The Direct Digitizer, REGIUS Model 110 is an X-ray image reader which uses a stimulable phosphor plate (Plate) as X-ray detector installed in a separate cassette, and reads the image recorded on the Plate by inserting a cassette in the entrance slot of this device. By means of laser scan and photoelectric method, this device reads the X-ray Image data created in form of a latent image on the Plate exposed by an external X-ray generating device, and converts the read data into digital. REGIUS Model 110 also reads the image
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data of long areas of anatomy and to verify the position for a radiotherapy location.
The Regius 110 is really just a minor modification of our 510k cleared Direct Digitizer, REGIUS Model 190, 510(k) number: K052095. The features in the Regius 110 that are different than the Regius 190 are minor and are features that are present in the 510k cleared Model DD341 / REGIUS150, 510(k) number: K0990359 which we have included on the Comparison Table.
The modification was made to the Regius 110 to achieve a more compact design. To achieve the compact design, the Maximum Image Matrix Size and Sampling Pitch are decreased from the Size and Pitch in the REGIUS Model 190 and the transport is slightly different. However, these differences are the same technology as found in the 510k cleared Model DD341 / REGIUS150.
Please refer to section 2, Substantial Equivalence Comparison Table for details. The basic operations of REGIUS Model 110 such as a starting, a shut down, a registration-of-patient, a setting of a various condition are operated with the optional Image Processing Work Station, REGIUS CONSOLE CS-2000/3000 (510(k) cleared, K051523, July 20, 2005) and so on. Then the image data transfer to an externally connected device such as a host computer, an order input device, an image display device, a printer, an image data filing device, and other image reproduction devices.
This device is not intended for use with digital mammography system.
#### 10. Intended Use
The Direct Digitizer, REGIUS Model 110 is an X-ray image reader which uses a stimulable phosphor plate (Plate) as X-ray detector installed in a separate cassette. It reads the image recorded on the Plate and transfers the image data to an externally connected device such as a host computer, an order input device, an image display device, a printer, an image data filing device, and other image reproduction devices. REGIUS Model 110 also reads the image data of long areas of anatomy and to verify the position for a radiotherapy location. It is designed and intended to be used by trained medical personnel in a clinic, a radiology department in a hospital and in other medical facilities. This device is not Intended for use with digital mammography system.
## 11. Substantial Equivalence to Predicate Device
The Direct Digitizer, REGIUS Model 110 is substantially equivalent to our Direct Digitizer REGIUS Model 190, 510(k) number: K052095. Comparison of the principal characteristics is shown in the Section 2.
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## 12. Compliance Standard
Safety standard : IEC60601-1 Ed.2(1988)+ A1(1991)+A2(1995) Electromagnetic Compatibility : IEC60601-1-2 Ed.2(2001)+A1(2004) Radiation safety : 21 CFR 1040.10, IEC60825-1(1993)+A1(1997)+A2:2001
## 13. Conclusion
The Direct Digitizer, REGIUS Model 110 has the same intended use and basically the same technological characteristic as the predicate device which is approved 510(k) number: K052095. This Special 510(k) has demonstrated substantial equivalence as the predicate device.
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Image /page/3/Picture/0 description: The image shows the logo for the Department of Health & Human Services. The logo includes a symbol on the left and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES" on the right. The symbol appears to be a stylized representation of a human figure or a caduceus. The text is in a clear, sans-serif font and is likely intended to convey the official nature of the organization.
Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room - WO66-G609 Silver Spring, MD 20993-0002
Konica Minolta Medical & Graphic, Inc. % Mr. Russell Munves Official Correspondent Storch, Amini & Munves, P.C. 140 East 45th Street, 25th Floor Two Grand Central Tower NEW YORK NY 10017
AUG 23 2013
Re: K071181
Trade/Device Name: Direct Digitizer. REGIUS Model 110 Regulation Number: 21 CFR 892.1680 Regulation Name: Stationary x-ray system Regulatory Class: II Product Code: MQB Dated: April 26, 2007 Received: April 30, 2007
Dear Mr. Munves:
This letter corrects our substantially equivalent letter of May 30. 2007.
We have reviewed your Section 510(k) premarket notification of intent to market the device we nave a viewed your ve 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 coninered phorts to May 20, 1976, tip 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. The I ou may, merciore, manel of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into class II (Special Controls), it may be subject to such If your device is Classified (see abor regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. 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 that I DA has made a could regulations administered by other Federal agencies. You must or any I catal statutes and regulanents, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Parts 801 and 809); medical device reporting (reporting of
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medical device-related adverse events) (21 CFR 803); and good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820). This letter will allow you to begin marketing your device as described in your Section 510(k) premarket whitiation. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Parts 801 and If you desire specific at 100 for your won Diagnostic Device Evaluation and Safety at (301) 796-007), program note the regulation entitled, "Misbranding by reference to premarket 5-156. Thise from 110.0 more 2019.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely Yours,
Janine M. Morris
Acting Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health
Enclosure
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## Indications for Use
510(k) Number (if known)
2671181
Device Name
Direct Digitizer, REGIUS Model 110
Indications for Use:
The Direct Digitizer, REGIUS Model 110 is an X-ray image reader which uses a stimulable phosphor plate (Plate) as X-ray detector installed in a separate cassette. It reads the image recorded on the Plate and transfers the image data to an externally connected device such as a host computer, an order input device, an image display device, a printer, an image data fillng device, and other image reproduction devices. REGIUS Model 110 also reads the image data of long areas of anatomy and to verify the position for a radiotherapy location. It is designed and Intended to be used by trained medical personnel In a clinic, a radiology department in a hospital and in other medical facilities. This device is not intended for use with digital mammography system
Prescription Use (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use ] (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF needed)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Huld Hensling
roductive, Abdominal, and
Page 1 of
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.
