510(k) K980985 ยท HNO Keratome, Ac-Powered
SCMD-1000
| Applicant | Howard Instruments, Inc., Tuscaloosa AL, US |
| Decision | Substantially Equivalent, May 1, 1998 |
| Received | Mar 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980985
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.