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

IMMUNOP. ANTIMITOCHONDRIAL ANTIBODY KIT

K Number: K800229 · Decision Feb 21, 1980
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
26
Applicant Total
30
Review Days
16

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Basic Information

Device Name
IMMUNOP. ANTIMITOCHONDRIAL ANTIBODY KIT
K Number
K800229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5090
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Clinical Sciences, Inc.
Date Received
February 5, 1980
Decision Date
February 21, 1980
Product Code
DBM
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DBM Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control

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K891990 RUBEOLA IGG CLIN-ELISA TEST SYSTEM, CAT. #4600
K883600 EPSTEIN-BARR VIRUS (EBNA-1) IGG CATA. #4550
K883601 EPSTEIN-BARR VIRUS (EBNA-1) IGM CATA. #5550
K874594 TOXOPLASMA IGM CLIN-ELISA(TM) CAT # 5560
K872942 IGM CMV CLIN-ELISA(TM) TEST SYSTEM NUMBER: 5530
K860145 RUBELLA ELISA TEST SYSTEM CATALOG NUMBER: 4540
K860773 TOXOPLASMA IGG CLIN-ELISA TEST KIT CAT. NO. 4560
Search all 30 clearances from Clinical Sciences, Inc. →