The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Immunoassay Control.
Device ID | K040379 |
510k Number | K040379 |
Device Name: | RANDOX IMMUNOASSAY CONTROL |
Classification | Multi-analyte Controls, All Kinds (assayed) |
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 | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-02-17 |
Decision Date | 2004-06-16 |