FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALBUMIN

K Number: K955781 · Decision Mar 13, 1996
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
119
Applicant Total
18
Review Days
83

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ALBUMIN
K Number
K955781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1035
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Derma Media Lab., Inc.
Date Received
December 21, 1995
Decision Date
March 13, 1996
Product Code
CIX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CIX Bromcresol Green Dye-Binding, Albumin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CIX), ordered by most recent decision date.

View all

Other Clearances by Derma Media Lab., Inc.

K Number Device Name
K971309 UREA
K970664 GLUCOSE REAGENT
K971072 CHOLESTEROL REAGENT
K971005 TRIGLYCERIDES
K970867 URIC ACID REAGENT
K964915 MAGNESIUM
K964913 IRON REAGENT
K965134 ALT/SGPT
K964914 ALKALINE PHOSPHATASE
K965126 AST/SGOT
Search all 18 clearances from Derma Media Lab., Inc. →