510(k) K921461 ยท GSS Antisera, Fluorescent, Pseudomonas Aeruginosa
TURKEL THORACENTESIS NEEDLE
| Applicant | Symbiosis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jul 30, 1992 |
| Received | Mar 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921461
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.