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

RUBELLA ANTIBODIES TEST REAGENTS

K Number: K810309 · Decision Mar 11, 1981
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
20
Applicant Total
41
Review Days
34

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Basic Information

Device Name
RUBELLA ANTIBODIES TEST REAGENTS
K Number
K810309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Calbiochem-Behring Corp.
Date Received
February 5, 1981
Decision Date
March 11, 1981
Product Code
GOL
Advisory Committee
Microbiology
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
GOL Antigen, Ha (Including Ha Control), Rubella

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Other Clearances by Calbiochem-Behring Corp.

K Number Device Name
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K830214 AFT SYSTEM III
K820812 CREATINE KINASE-MB KIT
K813493 ENZYGNOST TM RUBELLA IGM
K820088 AFT SYSTEM PROFICIENCY TESTING PROGRAM
K812458 PADAC
K810718 C-PEPTICE REAGENTS
K810669 PANTRAK E.K.
K810404 RHEUMATOID FACTORS REFERENCE SERUM
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