510(k) K791241 ยท JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
BRIOX MODEL 2000-CA COMPRESSOR UNIT
| Applicant | Briox Technologies, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 24, 1979 |
| Received | Jul 6, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791241
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.