510(k) K974606 ยท JGJ Photometric Method, Magnesium
RANDOX MAGNESIUM
| Applicant | Randox Laboratories, Ltd., Crumlin, Co. Antrim, IE |
| Decision | Substantially Equivalent, Feb 12, 1998 |
| Received | Dec 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974606
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 13, 2020 | Randox Laboratories Ltd. Randox Mg R1 - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine
Catalogue Number: MG3880 Terminated |
JGJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.