510(k) K984119 ยท CFM Bathophenanthroline, Colorimetry, Iron (Non-Heme)
WAKO L-TYPE FE, WAKO L-TYPE CALIBRATOR
| Applicant | Wako Chemicals USA, Inc., Richmond VA, US |
| Decision | Substantially Equivalent, Jan 15, 1999 |
| Received | Nov 18, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984119
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.