The following data is part of a premarket notification filed by Randox Laboratories Limited with the FDA for Randox Liquid Cardiac Control Levels 1, 2 And 3.
| Device ID | K110534 |
| 510k Number | K110534 |
| Device Name: | RANDOX LIQUID CARDIAC CONTROL LEVELS 1, 2 AND 3 |
| Classification | Multi-analyte Controls, All Kinds (assayed) |
| Applicant | RANDOX LABORATORIES LIMITED 55 DIAMOND ROAD CRUMLIN Crumlin Antrim, GB Bt29 4qy |
| Contact | Pauline Armstrong |
| Correspondent | Pauline Armstrong RANDOX LABORATORIES LIMITED 55 DIAMOND ROAD CRUMLIN 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 | 2011-02-25 |
| Decision Date | 2012-01-23 |