510(k) K923872 ยท GDM Needle, Aspiration And Injection, Reusable
BONE MARROW BIOPSY SYSTEM
| Applicant | The Straumann Co., Cambridge MA, US |
| Decision | Substantially Equivalent, Dec 15, 1992 |
| Received | Aug 3, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923872
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.