Retinalabs.Com is one of 25974 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Retinalabs.Com - FDA 510(k) Cleared Devices
Recent clearances: TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025, PDT DOSECALCULATOR, MODEL 80000, VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES
5
Total
5
Cleared
0
Denied
Retinalabs.Com has 5 FDA 510(k) cleared medical devices. Based in Atlanta, US.
Historical record: 5 cleared submissions from 2000 to 2000. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Retinalabs.Com Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Retinalabs.Com
5 devices
Cleared
Dec 22, 2000
TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL...
Ophthalmic
84d
Cleared
Oct 24, 2000
PDT DOSECALCULATOR, MODEL 80000
General Hospital
259d
Cleared
May 09, 2000
VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES
Ophthalmic
88d
Cleared
May 08, 2000
TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001
Ophthalmic
90d
Cleared
May 08, 2000
SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003
Ophthalmic
90d