The following data is part of a premarket notification filed by Diagnostic Chemicals Ltd. with the FDA for Uric Acid-sl Assay Catalogue No. 237-60.
Device ID | K961586 |
510k Number | K961586 |
Device Name: | URIC ACID-SL ASSAY CATALOGUE NO. 237-60 |
Classification | Acid, Uric, Uricase (colorimetric) |
Applicant | DIAGNOSTIC CHEMICALS LTD. WEST ROYALTY INDUSTRIAL PARK, Charlottetown, P.e.i., CA C1e 2a6 |
Contact | Karen Callbeck |
Correspondent | Karen Callbeck DIAGNOSTIC CHEMICALS LTD. WEST ROYALTY INDUSTRIAL PARK, Charlottetown, P.e.i., CA C1e 2a6 |
Product Code | KNK |
CFR Regulation Number | 862.1775 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-04-24 |
Decision Date | 1996-07-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00628063401000 | K961586 | 000 |
00628063400997 | K961586 | 000 |