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

LEGIONELLA STAT IGG/IGM TEST KIT

K Number: K911356 · Decision Jul 30, 1992
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
9
Applicant Total
30
Review Days
490

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Basic Information

Device Name
LEGIONELLA STAT IGG/IGM TEST KIT
K Number
K911356
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3300
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Whittaker Bioproducts, Inc.
Date Received
March 28, 1991
Decision Date
July 30, 1992
Product Code
MJH
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
MJH Legionella, Spp., Elisa

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Other Clearances by Whittaker Bioproducts, Inc.

K Number Device Name
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
K894932 FIAX EB VCA-M TEST KIT
K894235 EB VCA STAT M TEST KIT
Search all 30 clearances from Whittaker Bioproducts, Inc. →