510(k) K893388 ยท BYE Attachment, Breathing, Positive End Expiratory Pressure
DEVILBISS MODEL 7351D REVITALIZER CPAP SYSTEM
| Applicant | Devilbiss Health Care, Inc., Somerset PA, US |
| Decision | Substantially Equivalent, Jun 23, 1989 |
| Received | May 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893388
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.