The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Methadone Assay.
Device ID | K040570 |
510k Number | K040570 |
Device Name: | RANDOX METHADONE ASSAY |
Classification | Enzyme Immunoassay, Methadone |
Applicant | RANDOX LABORATORIES, LTD. 55 DIAMOND RD. Crumlin, County Antrim, GB Bt29 4qy |
Contact | Pauline Armstrong |
Correspondent | Pauline Armstrong RANDOX LABORATORIES, LTD. 55 DIAMOND RD. Crumlin, County Antrim, GB Bt29 4qy |
Product Code | DJR |
CFR Regulation Number | 862.3620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-03-04 |
Decision Date | 2004-05-10 |