FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RUBEOLA IGG CLIN-ELISA TEST SYSTEM, CAT. #4600

K Number: K891990 · Decision Jun 15, 1989
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
30
Review Days
79

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Basic Information

Device Name
RUBEOLA IGG CLIN-ELISA TEST SYSTEM, CAT. #4600
K Number
K891990
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3520
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Clinical Sciences, Inc.
Date Received
March 28, 1989
Decision Date
June 15, 1989
Product Code
LJB
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
LJB Enzyme Linked Immunoabsorbent Assay, Rubeola Igg

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LJB), 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
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
K854666 CYTOMEGALOVIRUS (CMV) ELISA TEST SYS. CAT. NO:4530
Search all 30 clearances from Clinical Sciences, Inc. →