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

FIAX EB VCA-M TEST KIT

K Number: K894932 · Decision Oct 16, 1989
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
55
Applicant Total
30
Review Days
74

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Basic Information

Device Name
FIAX EB VCA-M TEST KIT
K Number
K894932
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3235
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Whittaker Bioproducts, Inc.
Date Received
August 3, 1989
Decision Date
October 16, 1989
Product Code
LSE
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
LSE Epstein-Barr Virus, Other

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Other Clearances by Whittaker Bioproducts, Inc.

K Number Device Name
K911356 LEGIONELLA STAT IGG/IGM TEST KIT
K913212 3M IGE SINGLE POINT FAST TEST
K904652 LYME STAT M TEST KIT
K904893 FIAX LYME M TEST KIT
K911473 EBNA STAT TEST KIT
K905468 PYLORI-G FIAX TEST KIT
K904738 PYLORI STAT TEST KIT
K901493 FITC MURINE MONOCLONAL ANTI-INFLUENZA TYPE B
K893579 FITC MURINE MONOCLONAL ANTI-INFLUENZA TYPE A
K894235 EB VCA STAT M TEST KIT
Search all 30 clearances from Whittaker Bioproducts, Inc. →