The following data is part of a premarket notification filed by Randox Laboratories Limited with the FDA for Randox Speciality Control (i) Levels 1, 2 And 3.
Device ID | K130337 |
510k Number | K130337 |
Device Name: | RANDOX SPECIALITY CONTROL (I) LEVELS 1, 2 AND 3 |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | RANDOX LABORATORIES LIMITED 55 DIAMOND ROAD Crumlin, Antrim, GB Bt29 4qy |
Contact | Pauline Armstrong |
Correspondent | Pauline Armstrong RANDOX LABORATORIES LIMITED 55 DIAMOND ROAD Crumlin, 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 | 2013-02-11 |
Decision Date | 2013-06-19 |
Summary: | summary |