Who is the manufacturer of Micro C Medical Imaging System, M01?

Oxos Medical, Inc. filed the 510(k) submission for Micro C Medical Imaging System, M01 (K211473).

What is the FDA product code for Micro C Medical Imaging System, M01?

IZL. It is classified under 21 CFR 892.1720 as a Class 2 device in the Radiology panel.

What is the regulatory pathway for Micro C Medical Imaging System, M01?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like Micro C Medical Imaging System, M01?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Micro C Medical Imaging System, M01

Q: What are the predicate devices for Micro C Medical Imaging System, M01?

Micro C Medical Imaging System, M01 (K203658).

K211473 · Oxos Medical, Inc. · IZL · Jun 4, 2021 · Radiology

Device Facts

Record ID	K211473
Device Name	Micro C Medical Imaging System, M01
Applicant	Oxos Medical, Inc.
Product Code	IZL · Radiology
Decision Date	Jun 4, 2021
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 892.1720
Device Class	Class 2
Attributes	Pediatric, 3rd-Party Reviewed

Intended Use

The M01 System is a hand-held X-ray system designed to aid clinicians with point of care visualization through diagnostic X-rays of extremities.

Device Story

Handheld, portable X-ray system for point-of-care diagnostic imaging of distal extremities. Comprises three subsystems: Emitter (X-ray tube, computer vision camera, operator controls), Cassette (digital X-ray detector, positioning lights), and Control Unit (high voltage generator, computing, display interface). Operator positions emitter over patient anatomy using computer vision positioning system; captures static/serial radiographs. System interfaces with external monitor, keyboard, mouse; supports PACS transfer. Used in clinical/surgical environments by trained clinicians. Provides diagnostic images to assist clinical decision-making. Benefits include portable, point-of-care visualization of extremities.

Clinical Evidence

No clinical data. Bench testing only, including usability testing for surgical environments and cleaning/disinfection validation.

Technological Characteristics

Handheld mobile X-ray system. Components: Emitter, Cassette (6x6" digital detector, Cesium Iodide scintillator), Control Unit. Energy: 120 VAC/60 Hz. Fixed mA (1.0), selectable kVp (40, 50, 60). Exposure times: 33ms, 66ms, 99ms. Connectivity: WiFi, Ethernet, USB 2.0, DICOM 3.0 compliant. Software: Custom validated, includes user interface for image adjustment (zoom, rotate, brightness, contrast, sharpness).

Indications for Use

Indicated for use by qualified/trained clinicians on adult and pediatric patients for taking diagnostic static and serial radiographic exposures of extremities. Not intended to replace radiographic systems with variable tube current and voltages (kVp) required for full optimization of image quality and radiation exposure for different exam types.

Regulatory Classification

Identification

A mobile x-ray system is a transportable device system intended to be used to generate and control x-ray for diagnostic procedures. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

Predicate Devices

Micro C Medical Imaging System, M01 (K203658)

Related Devices

K203658 — Micro C Medical Imaging System, M01 · Oxos Medical, Inc. · Jan 12, 2021
K193535 — EZER, Portable X-ray System · Livermoretech, Inc. · May 7, 2020
K212654 — Micro C Medical Imaging System, M01 · Oxos Medical, Inc. · Feb 4, 2022
K230581 — TOPA12 Portable X-ray Unit · Neuf, Inc. · Aug 16, 2023
K252068 — MC2 Portable X-ray System · Oxos Medical · Dec 22, 2025

Submission Summary (Full Text)

{0}------------------------------------------------ June 4, 2021 Image /page/0/Picture/1 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. OXOS Medical, Inc. % Prithul Bom Most Responsible Person Regulatory Technology Services, LLC 1000 Westgate Drive. Suite 510k SAINT PAUL MN 55114 Re: K211473 Trade/Device Name: Micro C Medical Imaging System, M01 Regulation Number: 21 CFR 892.1720 Regulation Name: Mobile x-ray system Regulatory Class: Class II Product Code: IZL Dated: May 11, 2021 Received: May 12, 2021 Dear Prithul Bom: 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 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 {1}------------------------------------------------ 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 (QS) 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 Thalia T. Mills, Ph.D. Director Division of Radiological Health OHT7: Office of In Vitro Diagnostics and Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K211473 Device Name Micro C Medical Imaging System, M01 #### Indications for Use (Describe) The Micro C Medical Imaging System, M01 is a handheld and portable general purpose X-ray system that is indicated for use by qualified/trained clinicians on adult and pediatric patients for taking diagnostic static and serial radiographic exposures of extremities. The device is not intended to replace a radiographic system that has both variable tube current and voltages (kVp) in the range that may be required for full optimization of image quality and radiation exposure for different exam types. Type of Use (Select one or both, as applicable) | <div> ☒ Prescription Use (Part 21 GER 801 Subpart D) </div> | <div> ☐ Over-The-Counter Use (21 CER 801 Subpart C) </div> | |----------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------| |----------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------| ## 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}------------------------------------------------ Image /page/3/Picture/2 description: The image shows the logo for OXOS Medical. The logo consists of four symbols: a circle with two gaps, an X, another circle with two gaps, and the letter S. Below the symbols, the word "MEDICAL" is written in a smaller font. # Section 5 510(k) Summary K211473 In accordance with 21 CFR §807.92 and the Safe Medical Devices Act of 1990, the following information is provided for the Micro C Medical Imaging System, M01 Traditional 510(k) premarket notification. The submission was prepared in accordance with the FDA guidance document, 'Format for Traditional and Abbreviated 510(k)s', issued on August 12, 2005. | Submitter: | OXOS Medical, Inc 1230 Peachtree St NE Suite #300 Atlanta, GA 30309 Tel: 1-855-SEE-XRAY | |---------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Submission Contact: | Mo Khosravanipour Director of Program Management OXOS Medical, Inc. Email: Mo@oxos.com | | | Grace Powers, MS, MBA, RAC Founder/Principal Consultant Powers Regulatory Consulting Email: grace@powersregulatory.com | | Submission Date: | April 16, 2021 | | Subject Device: | Trade Name: Micro C Medical Imaging System, M01 Common Name: System, X-Ray, Mobile Regulation: 21 CFR § 892.1720 Regulatory Classification: 2 Product Code: IZL Classification Panel: Radiology | | Predicate Device: | Legally marketed device to which substantial equivalence is claimed: Micro C Medical Imaging System, M01 (K203658) Common Name: System, X-Ray, Mobile Regulation: 21 CFR § 892.1720 Regulatory Classification: 2 Product Code: IZL Classification Panel: Radiology | {4}------------------------------------------------ ## Section 5 510(k) Summary ## Device Description: The Micro C Medical Imaging System, M01 (subject device) is a handheld X-ray system designed to aid clinicians with point of care visualization through diagnostic X-rays of distal extremities. The device allows a clinician to select desired technique factors best suited for their patient anatomy. The Micro C Medical Imaging System, M01 consists of three major subsystems: The Emitter, Cassette, and Control Unit. The System is intended to interface an external Monitor (touchscreen or non-touchscreen display), keyboard and a mouse, and can provide a remote operator interface over the network to a laptop. The Micro C Medical Imaging System, M01 utilizes a computer vision positioning system to allow the emitter to be positioned above the patient anatomy and aligned to the cassette by the operator. The device is used in a clinical environment. A description of the three major sub-systems is listed below. - Emitter: This component contains the operator control panel, X-ray tube, and computer vision camera. The control panel allows the operator to control the major functions of the device, including the technique factors. This component is controlled and held in the operator's hand. - Cassette: This component contains the X-ray detector that collects the X-ray energy and provides a digital representation to the control unit for eventual display. This component also contains status lights and IR lights to assist in X-ray field positioning. The patient anatomy of interest is placed on top of this module. - . Control Unit: This component contains the High Voltage generator, computing power, monitor and keyboard inputs, and other electronics required for the functioning of the device. This module is typically placed on a shelf, cart, counter, or other flat surface convenient to the operator and environment. The system is intended to work in conjunction with a DICOM monitor, keyboard and a mouse and the mains power outlet. These are accessories are not included in the submission. The Micro C Medical Imaging System, M01 has custom validated software that includes a user interface that allows the operator to view and adjust captured radiographs and transfer radiographs to a PACS server or flash drive. The device software is based on the predicate device and no changes to the software were performed for this submission. Image /page/4/Figure/9 description: The image shows a white box connected to a white handheld device and a white square device via cables. Two blue cables connect the box to the handheld device and the square device. A gray cable connects the box to the square device. ## Figure 5-1: Subject Device - Micro C Medical Imaging System, M01 {5}------------------------------------------------ Image /page/5/Picture/2 description: The image shows a computer setup with a monitor, keyboard, mouse, and a white box-shaped device. The monitor is connected to the white box, which also has connections for the keyboard, mouse, and an Ethernet cable. The power cords for the monitor and the white box are plugged into wall outlets. ## Intended Use: The M01 System is a hand-held X-ray system designed to aid clinicians with point of care visualization through diagnostic X-rays of extremities. ## Indications for Use: The Micro C Medical Imaging System, M01 is a handheld and portable general purpose X-ray system that is indicated for use by qualified/trained clinicians on adult and pediatric patients for taking diagnostic static and serial radiographic exposures of extremities. The device is not intended to replace a radiographic system that has both variable tube current and voltages (kVp) in the range that may be required for full optimization of image quality and radiation exposure for different exam types. ## Technological Characteristics The Micro C Medical Imaging System, M01 is identical to the predicate device cleared via K203658. The purpose of this submission is to add the pediatric population to the indication and to allow use in surgery. The table below compares the subject and predicate device. | | | Comparison | | |-----------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------| | Subject Device: Micro C Medical Imaging System, M01 | Predicate Device: Micro C Medical Imaging System, M01 (K203658) | | | | Product Code | IZL (Mobile X-Ray System) | IZL (Mobile X-Ray System) | Identical | | Regulation | 21 CFR 892.1720 | 21 CFR 892.1720 | Identical | | Classification Name | Mobile X-Ray System | Mobile X-Ray System | Identical | | Classification | Class 2 | Class 2 | Identical | | Indication for Use | The Micro C Medical Imaging System, M01 is a handheld and portable general purpose X-ray system that is indicated | The Micro C Medical Imaging System, M01 is a handheld and portable general purpose X-ray system | Different- The subject device can be used in pediatric populations. | | | for use by qualified/trained clinicians on adult patients for taking diagnostic static and serial radiographic exposures of extremities. The device is not intended to replace a radiographic system that has both variable tube current and voltages (kVp) in the range that may be required for full optimization of image quality and radiation exposure for different exam types. | that is indicated for use by qualified/trained clinicians on adult and pediatric patients for taking diagnostic static and serial radiographic exposures of extremities. The device is not intended to replace a radiographic system that has both variable tube current and voltages (kVp) in the range that may be required for full optimization of image quality and radiation exposure for different exam types. | | | Age of Device Use | Adults and Pediatric | Adults | Different- The subject device can be used in pediatric populations. | | Principle of Operation | General purpose diagnostic X-ray | General purpose diagnostic X-ray | Identical | | Image type produced | Static, serial radiographic and photographic images for convenience. | Static, serial radiographic and photographic images for convenience. | Identical | | Detector | 6 x 6" digital detector | 6 x 6" digital detector | Identical | | Collimator | The removable fixed collimators (referred to as pucks) | The removable fixed collimators (referred to as pucks) | Identical | | Weight | Emitter: 2.86kg (6.3lbs) Cassette: 6.5kg (14.3lbs) Control Unit: 8.6kg (19.0lbs) | Emitter: 2.86kg (6.3lbs) Cassette: 6.5kg (14.3lbs) Control Unit: 8.6kg (19.0lbs) | Identical | | Dimension/ Size | Emitter: 9.3"H x 3.5"W x 8.3"L (excluding SSD Cone) Cassette: 15.5"H x 15.5"W x 2.8"L Control Unit: 16.4"H x 12.9"W x 5.5"L | Emitter: 9.3"H x 3.5"W x 8.3"L (excluding SSD Cone) Cassette: 15.5"H x 15.5"W x 2.8"L Control Unit: 16.4"H x 12.9"W x 5.5"L | Identical | | Triggering Mechanism | Two stage triggering | Two stage triggering | Identical | | Minimum Source to skin distance (SSD) | 20 cm SSD Cone ensures minimum SSD of 20 cm | 20 cm SSD Cone ensures minimum SSD of 20 cm | Identical | | Source to Detector distance | 20 - 45 cm | 20 - 45 cm | Identical | | Light Field | Virtual light field on Monitor UI. No projected light field. | Virtual light field on Monitor UI. No projected light field. | Identical | | Energy Source | 120 VAC / 60 Hz (no rechargeable battery) | 120 VAC / 60 Hz (no rechargeable battery) | Identical | | Exposure Time | 33ms, 66ms and 99ms | 33ms, 66ms and 99ms | Identical | | mA | 1.0 mA fixed | 1.0 mA fixed | Identical | | kVp | 40kVp, 50kVp, and 60kVp | 40kVp, 50kVp, and 60kVp | Identical | | Scintillator | Cesium lodide (CsI) | Cesium lodide (CsI) | Identical | | Resolution/ Pixel size | 99 μm | 99 μm | Identical | | DQE @ 0Lp/mm | 70% | 70% | Identical | | MTF @ 1 Lp/mm, RQA5 | 60% | 60% | Identical | | Ingress Protection Rating | IPOO | IPOO | Identical | | Image Processing | User Interface can be used to drag, zoom, rotate and also adjust brightness, contrast, and sharpness. | User Interface can be used to drag, zoom, rotate and also adjust brightness, contrast, and sharpness. | Identical | | Connectivity Options | WiFi, Ethernet, Four USB 2.0 ports | WiFi, Ethernet, Four USB 2.0 ports | Identical | | DICOM | Yes- DICOM 3.0 Compliant | Yes- DICOM 3.0 Compliant | Identical | | Device Package Contents | ● Cassette ● Control Unit ● Emitter ● Collimation Pucks ● SSD Cone ● Cassette Power Cable ● Cassette Data Cable ● Control Unit Power Cable | ● Cassette ● Control Unit ● Emitter ● Collimation Pucks ● SSD Cone ● Cassette Power Cable ● Cassette Data Cable ● Control Unit Power Cable | Identical | | | Connector Covers Instructions for Use Case | Connector Covers Instructions for Use Case | | ## Table 5-2: Device Comparison {6}------------------------------------------------ {7}------------------------------------------------ {8}------------------------------------------------ #### Non-Clinical Performance Data Testing specific to the use in surgery was performed and includes: - Usability testing for use in surgery - Cleaning and Disinfection Studies ● The following specific guidance document was utilized in the device development to ensure the safety of this device for both the operators and patients: - Guidance for Medical X-ray Imaging Devices Conformance with IEC Standards ● - . Guidance for the Submission of 510(k)s for Solid State X-ray Imaging Devices - Radiation Safety Considerations for X-ray Equipment Designed for Hand-held Use - Pediatric Information for X-ray Imaging Device Premarket Notifications #### Conclusion The Micro C Medical Imaging System, M01 is identical in design to the legally marketed predicate device. The updated indication and contraindication are acceptable as demonstrated by the performance data and does not raise different questions of safety and effectiveness.