Retinalabs.Com
Atlanta, GA, US
Retinalabs.Com appears in FDA device records in Atlanta, GA. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Retinalabs.Com in 2000.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K003036 | TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025 | KYG | Substantially Equivalent | |
| K000418 | PDT DOSECALCULATOR, MODEL 80000 | NDC | Substantially Equivalent | |
| K000457 | VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES | HMX | Substantially Equivalent | |
| K000420 | SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003 | MRH | Substantially Equivalent | |
| K000416 | TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001 | MPA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain