The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Barbiturate Assay.
Device ID | K041143 |
510k Number | K041143 |
Device Name: | RANDOX BARBITURATE 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 |
CFR Regulation Number | 862.3150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-04-30 |
Decision Date | 2004-11-05 |