The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Carbamazepine.
Device ID | K011648 |
510k Number | K011648 |
Device Name: | RANDOX CARBAMAZEPINE |
Classification | Enzyme Immunoassay, Carbamazepine |
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 | KLT |
CFR Regulation Number | 862.3645 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-05-29 |
Decision Date | 2002-01-15 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05055273206463 | K011648 | 000 |