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

WAKO IMMUNOASSAY CALIBRATOR SET

K Number: K010332 · Decision Aug 1, 2001
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
244
Applicant Total
121
Review Days
180

Basic Information

Device Name
WAKO IMMUNOASSAY CALIBRATOR SET
K Number
K010332
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WAKO CHEMICALS, USA, INC.
Date Received
February 2, 2001
Decision Date
August 1, 2001
Product Code
JIT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JIT Calibrator, Secondary

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