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

TOXOPLASMA IGG CLIN-ELISA TEST KIT CAT. NO. 4560

K Number: K860773 · Decision May 23, 1986
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
30
Review Days
81

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Basic Information

Device Name
TOXOPLASMA IGG CLIN-ELISA TEST KIT CAT. NO. 4560
K Number
K860773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Clinical Sciences, Inc.
Date Received
March 3, 1986
Decision Date
May 23, 1986
Product Code
LGD
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

Similar 510(k) Clearances

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

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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
K854666 CYTOMEGALOVIRUS (CMV) ELISA TEST SYS. CAT. NO:4530
Search all 30 clearances from Clinical Sciences, Inc. →