510(k) K961380 ยท GEX Powered Laser Surgical Instrument
CPC PROBE
| Applicant | Carl Zeiss, Inc., Thornwood NY, US |
| Decision | Substantially Equivalent, Mar 17, 1997 |
| Received | Apr 10, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961380
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.