The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Maternal Control, Levels 1, 2 And 3.
| Device ID | K113720 |
| 510k Number | K113720 |
| Device Name: | RANDOX MATERNAL CONTROL, LEVELS 1, 2 AND 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 | 2011-12-19 |
| Decision Date | 2012-09-20 |
| Summary: | summary |