510(k) K803232 ยท CAW Generator, Oxygen, Portable
COMPRESSED AIR & OXYGEN GEN./DELIVERY SY
| Applicant | Dri-Aire, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 2, 1981 |
| Received | Dec 22, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803232
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.