510(k) K953642 ยท JEH Plethysmograph, Volume
AP-18
| Applicant | Jeneric/Pentron, Inc., Wallingford CT, US |
| Decision | Substantially Equivalent, Dec 12, 1995 |
| Received | Aug 4, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953642
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.