The following data is part of a premarket notification filed by Em Diagnostic Systems, Inc. with the FDA for Abbott Quickstart Albumin Test (albg) Item #5a37.
Device ID | K913920 |
510k Number | K913920 |
Device Name: | ABBOTT QUICKSTART ALBUMIN TEST (ALBG) ITEM #5A37 |
Classification | Bromcresol Green Dye-binding, Albumin |
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 | CIX |
CFR Regulation Number | 862.1035 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-09-03 |
Decision Date | 1991-09-27 |