The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Methamphetamine Assay.
| Device ID | K092266 |
| 510k Number | K092266 |
| Device Name: | RANDOX METHAMPHETAMINE ASSAY |
| Classification | Calibrators, Drug Mixture |
| Applicant | RANDOX LABORATORIES, LTD. 55 DIAMOND RD. Crumlin, County Antrim, GB Bt29 4qy |
| Contact | P Armstrong |
| Correspondent | P Armstrong RANDOX LABORATORIES, LTD. 55 DIAMOND RD. Crumlin, County Antrim, GB Bt29 4qy |
| Product Code | DKB |
| Subsequent Product Code | DIF |
| Subsequent Product Code | LAF |
| CFR Regulation Number | 862.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-07-28 |
| Decision Date | 2011-05-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05055273208009 | K092266 | 000 |
| 05055273207903 | K092266 | 000 |
| 05055273207897 | K092266 | 000 |
| 05055273207880 | K092266 | 000 |