510(k) K885075 ยท EIL Gauge, Depth, Instrument, Dental
ABIOMED PERIOTEMP(TM) PROBE
| Applicant | Abiomed, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Feb 13, 1989 |
| Received | Dec 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885075
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.