The following data is part of a premarket notification filed by Randox Laboratories, Ltd. with the FDA for Randox Urine Controls.
Device ID | K043266 |
510k Number | K043266 |
Device Name: | RANDOX URINE CONTROLS |
Classification | Urinalysis Controls (assayed And Unassayed) |
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 | JJW |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-11-26 |
Decision Date | 2005-02-15 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05055273200546 | K043266 | 000 |
05055273200539 | K043266 | 000 |