The following data is part of a premarket notification filed by Clarity Medical Systems with the FDA for Retcam 3 Opthalmic Imaging System.
Device ID | K102859 |
510k Number | K102859 |
Device Name: | RETCAM 3 OPTHALMIC IMAGING SYSTEM |
Classification | Camera, Ophthalmic, Ac-powered |
Applicant | CLARITY MEDICAL SYSTEMS 5775 WEST LAS POSITAS BLVD. SUITE 200 Pleasanton, CA 94588 -4084 |
Contact | Gary A Seeger |
Correspondent | Gary A Seeger CLARITY MEDICAL SYSTEMS 5775 WEST LAS POSITAS BLVD. SUITE 200 Pleasanton, CA 94588 -4084 |
Product Code | HKI |
CFR Regulation Number | 886.1120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-30 |
Decision Date | 2011-04-20 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00899281002113 | K102859 | 000 |