The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Evidence.
Device ID | K030360 |
510k Number | K030360 |
Device Name: | RANDOX EVIDENCE |
Classification | Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
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 | DIO |
Subsequent Product Code | DLJ |
Subsequent Product Code | JJE |
CFR Regulation Number | 862.3250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-02-03 |
Decision Date | 2003-12-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05055273214024 | K030360 | 000 |
05055273202694 | K030360 | 000 |
05055273202663 | K030360 | 000 |
05055273202656 | K030360 | 000 |
05055273202458 | K030360 | 000 |
05055273202397 | K030360 | 000 |
05055273202335 | K030360 | 000 |
05055273202137 | K030360 | 000 |