510(k) K935179

EMDS ALBUMIN (ALB) TEST by Em Diagnostic Systems, Inc. — Product Code CIX

K935179 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "EMDS ALBUMIN (ALB) TEST". The FDA issued a decision of Substantially Equivalent on December 17, 1993. The device falls under product code CIX (Bromcresol Green Dye-Binding, Albumin), a Class II device regulated under 21 CFR 862.1035. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 17, 1993
Date Received
October 26, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bromcresol Green Dye-Binding, Albumin
Device Class
Class II
Regulation Number
862.1035
Review Panel
CH
Submission Type