510(k) K922817 ยท KDP Regulator, Vacuum
PM3000 & PM3100 VACUUM REGULATOR
| Applicant | Precision Medical, Inc., Northampton PA, US |
| Decision | Substantially Equivalent, Mar 4, 1993 |
| Received | Jun 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922817
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.