The following data is part of a premarket notification filed by Em Diagnostic Systems, Inc. with the FDA for Abbott Quickstart Uric Acid Test (urca) Item# 5a34.
Device ID | K913706 |
510k Number | K913706 |
Device Name: | ABBOTT QUICKSTART URIC ACID TEST (URCA) ITEM# 5A34 |
Classification | Acid, Uric, Uricase (colorimetric) |
Applicant | EM DIAGNOSTIC SYSTEMS, INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Contact | Anna G Bentley |
Correspondent | Anna G Bentley EM DIAGNOSTIC SYSTEMS, INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Product Code | KNK |
CFR Regulation Number | 862.1775 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-19 |
Decision Date | 1991-09-27 |