510(k) K801349 ยท JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
LOSEFF BALLOON TYPE SELF-RETENTION WOUND
| Applicant | Loseff Medical Designers, Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 7, 1980 |
| Received | Jun 9, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801349
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.