(450 days)
Not Found
Not Found
No
The provided 510(k) summary contains no mention of AI, ML, or related concepts like deep neural networks, image processing (in a way that suggests AI), or performance metrics typically associated with AI/ML models (AUC, sensitivity, specificity, etc.). The description is limited to the intended use and anatomical site, which are standard for ophthalmic imaging devices and do not inherently imply AI/ML.
No
The device is described for "imaging, visualization, and fluorescein angiography," which are diagnostic rather than therapeutic functions.
No
The device is described as being for "general ophthalmic imaging, visualization, and fluorescein angiography." While these can be inputs to a diagnostic process, the description does not state that the device itself performs diagnosis (e.g., identifying disease, classifying conditions, or making a diagnostic judgment). It focuses on data acquisition for observation.
Unknown
The provided 510(k) summary lacks a device description, making it impossible to determine if the device is software-only or includes hardware components.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for "general ophthalmic imaging, visualization, and fluorescein angiography including anterior and posterior segments of the eye." This describes a device used to image the eye, not to perform tests on samples taken from the body (like blood, urine, or tissue).
- Lack of IVD Characteristics: The description doesn't mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples.
- Detecting or measuring substances in samples.
- Providing information for diagnosis based on laboratory tests.
This device appears to be an ophthalmic imaging device, which falls under a different regulatory category than IVDs.
N/A
Intended Use / Indications for Use
For general ophthalmic imaging, visualization, and fluorescein angiography including anterior and posterior segments of the eye.
Product codes
MXK
Device Description
Not Found
Mentions image processing
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Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
anterior and posterior segments of the eye
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Not Found
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 886.1850 AC-powered slitlamp biomicroscope.
(a)
Identification. An AC-powered slitlamp biomicroscope is an AC-powered device that is a microscope intended for use in eye examination that projects into a patient's eye through a control diaphragm a thin, intense beam of light.(b)
Classification. Class II (special controls). The device, when it is intended only for the visual examination of the anterior segment of the eye, is classified as Group 1 per FDA-recognized consensus standard ANSI Z80.36, does not provide any quantitative output, and is not intended for screening or automated diagnostic indications, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 886.9.
0
DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three stripes representing human services. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
SEP - 2 2004
Massie Research Laboratories, Inc. c/o N.A. (Bert) Massie, Ph.D. 5775 W. Las Positas Blvd Suite 200 Pleasanton, CA 94588-4084
Re: K031788
Trade/Device Name: Anterior Segment Analysis Device Regulation Number: 21 CFR 886.1850 Regulatory Class: Class II Product Code: MXK Dated: July 31, 2004 Received: August 2, 2004
Dear Mr. Massie:
We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviewed your bection of the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use stated in the Clerosury to regars actuent date of the Medical Device Amendments, or to commerce price to May 20, 1976, the excordance with the provisions of the Federal Food, Drug, devices that have been recuire approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The You may, therefore, market the device, Books requirements for annual registration, listing of general controls provisions of ractice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it If your device is classified (800 a0070) als. Existing major regulations affecting your device can thay be subject to suen additions, Title 21, Parts 800 to 898. In addition, FDA may be found in the Oucements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean I loast be devised that i Dr rivetion that your device complies with other requirements of the Act that I DA has made a acterialized administered by other Federal agencies. You must of any I edelin Statutes and regurements, including, but not limited to: registration and listing compry with and 100 recess requirements Part 801); good manufacturing practice requirements as set (21 CFR Part 807), accems (QS) regulation (21 CFR Part 820); and if applicable, the electronic form in the quant) byevelles (Sections 531-542 of the Act); 21 CFR 1000-1050.
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Page 2- N.A. (Bert) Massie, Ph.D.
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. 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 Part 801), please contact the Office of Compliance at (301) 594-4613. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). 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) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
Alegi Rosenthal
A. Ralph Rosenthal, M.D. Director Division of Ophthalmic and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
K031788 510(k) Number :
Device Name:
Pathfinder or other to be determined
Indications for use:
For general ophthalmic imaging, visualization, and fluorescein angiography including anterior and posterior segments of the eye.
Prescription Use X (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)
Sean L Keefe
(Division Sign-Off) Division of Ophthalmic Ear, Nose and Throat Devises
510(k) Number_________________________________________________________________________________________________________________________________________________________________