510(k) K002831 ยท CAF Nebulizer (Direct Patient Interface)
VEGA ULTRASONIC NEBULIZER
| Applicant | Vega Technologies, Inc., Taipei, TW |
| Decision | Substantially Equivalent, May 23, 2001 |
| Received | Sep 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002831
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.