510(k) K162200 ยท JGJ Photometric Method, Magnesium
Randox RX Daytona Plus Magnesium (MG)
| Applicant | Randox Laboratories, Ltd., Crumlin, GB |
| Decision | Substantially Equivalent, Apr 28, 2017 |
| Received | Aug 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162200
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 13, 2020 | Randox Laboratories Ltd. Randox Rx Series Mg - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine
Catalogue Number: MG8326 Terminated |
JGJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.