The following data is part of a premarket notification filed by Em Diagnostic Systems, Inc. with the FDA for Cholesterol Test Item# 42374/93, 42322/r1.
Device ID | K924508 |
510k Number | K924508 |
Device Name: | CHOLESTEROL TEST ITEM# 42374/93, 42322/R1 |
Classification | Enzymatic Esterase--oxidase, Cholesterol |
Applicant | EM DIAGNOSTIC SYSTEMS, INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Contact | Carol Faulkner |
Correspondent | Carol Faulkner EM DIAGNOSTIC SYSTEMS, INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Product Code | CHH |
CFR Regulation Number | 862.1175 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-04 |
Decision Date | 1993-01-28 |