510(k) K954448 ยท FRA Purifier, Air, Ultraviolet, Medical
VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM
| Applicant | Schiff & Co., West Cadwell NJ, US |
| Decision | Substantially Equivalent, Oct 28, 1996 |
| Received | Sep 25, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954448
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.