510(k) K912892 ยท KNW Instrument, Biopsy
AUTO-VAC BIOPSY NEEDLE
| Applicant | Angiomed GmbH & Co. Medizintechnik KG, Germany, DE |
| Decision | Substantially Equivalent, Feb 7, 1992 |
| Received | Jul 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912892
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.