510(k) K960944 ยท CAD Vaporizer, Anesthesia, Non-Heated
PPV VAPORIZER (MODIFICATION)
| Applicant | Penlon , Ltd., Oxonn, GB |
| Decision | Substantially Equivalent, Apr 2, 1996 |
| Received | Feb 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960944
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.