510(k) K884090 ยท CAD Vaporizer, Anesthesia, Non-Heated
LUNDY VAPORIZER SYSTEM
| Applicant | Vaporflow Technology, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Jan 24, 1989 |
| Received | Sep 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884090
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.