510(k) K011488 ยท HFB Forceps, Biopsy, Gynecological
SPIRABRUSH CX BIOPSY INSTRUMENT
| Applicant | Trylon Corp., Torrance CA, US |
| Decision | Substantially Equivalent, Feb 22, 2002 |
| Received | May 15, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011488
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.