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

TXOCELL-IHA REAGENT SYSTEM

K Number: K790460 · Decision May 25, 1979
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
7
Applicant Total
41
Review Days
81

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Basic Information

Device Name
TXOCELL-IHA REAGENT SYSTEM
K Number
K790460
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Calbiochem-Behring Corp.
Date Received
March 5, 1979
Decision Date
May 25, 1979
Product Code
GMM
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
GMM Antigens, Iha, Toxoplasma Gondii

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K Number Device Name
K831811 REVOLUTION RADIAL IMMUNODIFFUSION PLATE
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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.
K810309 RUBELLA ANTIBODIES TEST REAGENTS
Search all 41 clearances from Calbiochem-Behring Corp. →