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

ROCHE DIAGNOSTICS INFLUENZA A/B RAPID TEST

K Number: K993048 · Decision Dec 20, 1999
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
71
Applicant Total
264
Review Days
101

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Basic Information

Device Name
ROCHE DIAGNOSTICS INFLUENZA A/B RAPID TEST
K Number
K993048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3328
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Roche Diagnostics Corp.
Date Received
September 10, 1999
Decision Date
December 20, 1999
Product Code
PSZ
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
PSZ Devices Detecting Influenza A, B, And C Virus Antigens

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