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

BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM

K Number: K965131 · Decision Mar 26, 1997
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
109
Applicant Total
12
Review Days
93

Basic Information

Device Name
BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM
K Number
K965131
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WAMPOLE LABORATORIES
Date Received
December 23, 1996
Decision Date
March 26, 1997
Product Code
LSR
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
LSR Reagent, Borrelia Serological Reagent

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