510(k) K923723 ยท HAO Instrument, Surgical, Non-Powered
SILICONE BRAIN SPATULA SET
| Applicant | Redmond Neurosurgical, Inc., Lake Zurich IL, US |
| Decision | Substantially Equivalent, Aug 12, 1992 |
| Received | Jul 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923723
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.