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

ANAZYME ANA PEROXIDASE TEST SYSTEM

K Number: K822911 · Decision Oct 22, 1982
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
4
Applicant Total
30
Review Days
21

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Basic Information

Device Name
ANAZYME ANA PEROXIDASE TEST SYSTEM
K Number
K822911
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Clinical Sciences, Inc.
Date Received
October 1, 1982
Decision Date
October 22, 1982
Product Code
DAA
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
DAA Igg, Peroxidase, Antigen, Antiserum, Control

Similar 510(k) Clearances

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Other Clearances by Clinical Sciences, Inc.

K Number Device Name
K900688 VARICELLA ZOSTER IGG CLIN-ELISA TEST KIT
K883870 EPSTEIN-BARR VIRAL CAPSID ANTIGEN IGG #4590
K883871 EPSTEIN-BARR VIRAL CAPSID ANTIGEN IGM #5590
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. →