The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Cannabinoids Asssay.
| Device ID | K041142 |
| 510k Number | K041142 |
| Device Name: | RANDOX CANNABINOIDS ASSSAY |
| Classification | Enzyme Immunoassay, Cannabinoids |
| 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 | LDJ |
| CFR Regulation Number | 862.3870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-04-30 |
| Decision Date | 2004-11-23 |
| Summary: | summary |