The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Albumin.
Device ID | K984494 |
510k Number | K984494 |
Device Name: | RANDOX ALBUMIN |
Classification | Bromcresol Green Dye-binding, Albumin |
Applicant | RANDOX LABORATORIES, LTD. ARDMORE, DIAMOND ROAD Crumlin, Co. Antrim, GB Bt29 4qy |
Contact | P Armstrong |
Correspondent | P Armstrong RANDOX LABORATORIES, LTD. ARDMORE, DIAMOND ROAD Crumlin, Co. Antrim, GB Bt29 4qy |
Product Code | CIX |
CFR Regulation Number | 862.1035 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-12-17 |
Decision Date | 1999-03-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05055273208115 | K984494 | 000 |
05055273200058 | K984494 | 000 |
05055273200041 | K984494 | 000 |