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FDA 510(k), K934880, MTI PHOTOSCREENER
FDA 510(k), K934880, MTI PHOTOSCREENER
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510(K) Number: K934880
Device Name: MTI PHOTOSCREENER
Manufacturer: MEDICAL TECHNOLOGY AND INNOVATIONS, INC.
Device Classification Name: photorefractor
Regulation Number: 886.1120
Classification Product Code: MMF
Date Received: 10/12/1993
Decision Date: 04/06/1994
Regulation Medical Specialty: Ophthalmic
Device Name: MTI PHOTOSCREENER
Manufacturer: MEDICAL TECHNOLOGY AND INNOVATIONS, INC.
Device Classification Name: photorefractor
Regulation Number: 886.1120
Classification Product Code: MMF
Date Received: 10/12/1993
Decision Date: 04/06/1994
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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