The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Bariturates Assay.
Device ID | K092268 |
510k Number | K092268 |
Device Name: | RANDOX BARITURATES ASSAY |
Classification | Enzyme Immunoassay, Barbiturate |
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 | DIS |
Subsequent Product Code | DLJ |
Subsequent Product Code | LAS |
CFR Regulation Number | 862.3150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-07-28 |
Decision Date | 2011-05-25 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05055273208016 | K092268 | 000 |