The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Phencyclidine Assay.
Device ID | K043071 |
510k Number | K043071 |
Device Name: | RANDOX PHENCYCLIDINE ASSAY |
Classification | Enzyme Immunoassay, Phencyclidine |
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 | LCM |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-11-08 |
Decision Date | 2005-01-27 |