510(k) K955781

ALBUMIN by Derma Media Lab., Inc. — Product Code CIX

K955781 is an FDA 510(k) premarket notification submitted by Derma Media Lab., Inc. for the device "ALBUMIN". The FDA issued a decision of Substantially Equivalent on March 13, 1996. The device falls under product code CIX (Bromcresol Green Dye-Binding, Albumin), a Class II device regulated under 21 CFR 862.1035. Derma Media Lab., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 13, 1996
Date Received
December 21, 1995
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