510(k) K920207 ยท GKG Centrifuge, Hematocrit
HERMLE Z230H
| Applicant | Labnet Intl., Inc., Woodbridge NJ, US |
| Decision | Substantially Equivalent, Jun 9, 1992 |
| Received | Jan 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920207
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.