510(k) K130282 ยท KNW Instrument, Biopsy
REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT
| Applicant | Remington Medical, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, May 13, 2013 |
| Received | Feb 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130282
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.