510(k) K012029 ยท KMG Purifier, Water, Ultraviolet, Medical
REMEDY MODEL 2Z12
| Applicant | Apollo Corp., Somerset WI, US |
| Decision | Substantially Equivalent, Dec 31, 2001 |
| Received | Jun 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012029
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.