510(k) K905232 ยท GEX Powered Laser Surgical Instrument
MOOR LASER BLOOD FLOW MONITOR MBF3
| Applicant | Moor Instruments, Ltd., Axminster, Devon, GB |
| Decision | Substantially Equivalent, Jan 11, 1991 |
| Received | Nov 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905232
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.