510(k) K896500 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
CWD/PPG MODULE
| Applicant | Life Sciences Manufacturing, Inc., West Lebanon NH, US |
| Decision | Substantially Equivalent, Jul 18, 1990 |
| Received | Nov 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896500
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.