The following data is part of a premarket notification filed by Em Diagnostic Systems, Inc. with the FDA for Abbott Quickstart Magnesium Test, Item #5a32.
Device ID | K913764 |
510k Number | K913764 |
Device Name: | ABBOTT QUICKSTART MAGNESIUM TEST, ITEM #5A32 |
Classification | Photometric Method, Magnesium |
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 | JGJ |
CFR Regulation Number | 862.1495 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-22 |
Decision Date | 1991-11-05 |