510(k) K790999 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
APOLLO HEART RATE INDICATOR
| Applicant | Apollo Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 22, 1979 |
| Received | May 29, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790999
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.