510(k) K954693 ยท FCK Instrument, Biopsy, Suction
MEHTA BRONCHIAL BIOSPY DRILL
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Oct 23, 1995 |
| Received | Oct 11, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954693
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.