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

HUMAN IGG-ALBUMIN TEST KIT

K Number: K811178 · Decision May 15, 1981
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
15
Review Days
17

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Basic Information

Device Name
HUMAN IGG-ALBUMIN TEST KIT
K Number
K811178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1035
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Meloy Laboratories, Inc.
Date Received
April 28, 1981
Decision Date
May 15, 1981
Product Code
CJQ
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
CJQ Radial Immunodiffusion, Albumin

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