510(k) K944479 ยท KDP Regulator, Vacuum
PM3300 INTERMITTENT VACUUM
| Applicant | Precision Medical, Inc., Northampton PA, US |
| Decision | Substantially Equivalent, Dec 22, 1994 |
| Received | Sep 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944479
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.