510(k) K952880 ยท CBK Ventilator, Continuous, Facility Use
MODEL LP-1000 VOLUME VENTILATOR
| Applicant | Aequitron Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jun 20, 1996 |
| Received | Jun 22, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952880
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.