510(k) K042648 ยท NON Forceps, Biopsy, Non-Electric, Reprocessed
REPROCESSED COLD BIOPSY FORCEPS
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 20, 2005 |
| Received | Sep 28, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042648
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 13, 2009 | Sterilmed Inc Biopsy Forceps, Cold
Model #'s:
BAR000386
BAR000388
MIC1012
MIC1331
MIC1333
MIC1337
MIC1536
MIC1589
MIC1597
MIC1598 and
MIC1599
The Reprocessed Cold Biopsy Forceps are intended to be used during endo Terminated |
NON | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.