Company ยท US
Retinalabs.Com
FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2000. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Dec 22, 2000 | K003036 | TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025 Retinalabs.Com | KYG |
| Oct 24, 2000 | K000418 | PDT DOSECALCULATOR, MODEL 80000 Retinalabs.Com | NDC |
| May 9, 2000 | K000457 | VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES Retinalabs.Com | HMX |
| May 8, 2000 | K000420 | SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003 Retinalabs.Com | MRH |
| May 8, 2000 | K000416 | TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001 Retinalabs.Com | MPA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||