510(k) K000048 ยท FMF Syringe, Piston
SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1
| Applicant | Biosurgical Corp., Pleasanton CA, US |
| Decision | Substantially Equivalent, Jan 31, 2000 |
| Received | Jan 7, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000048
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.