510(k) K880101 ยท BYJ Unit, Liquid-Oxygen, Portable
LIBERATOR 53/STROLLER 50
| Applicant | Minnesota Valley Engineering, Inc., New Prague MN, US |
| Decision | Substantially Equivalent, Feb 29, 1988 |
| Received | Jan 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880101
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.