510(k) K043523 ยท KNW Instrument, Biopsy
INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE
| Applicant | Medical Device Technologies, Inc., Wheeling IL, US |
| Decision | Substantially Equivalent, Feb 11, 2005 |
| Received | Dec 20, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043523
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.