The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Immunoassay Speciality Control (ii), Level 1, Level 2 And Level 3.
Device ID | K121603 |
510k Number | K121603 |
Device Name: | RANDOX IMMUNOASSAY SPECIALITY CONTROL (II), LEVEL 1, LEVEL 2 AND LEVEL 3 |
Classification | Multi-analyte Controls, All Kinds (assayed) |
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 | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-04-06 |
Decision Date | 2012-11-20 |
Summary: | summary |