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

GENZYME DIRECT AMYLASE VERIFIER

K Number: K993132 · Decision Oct 4, 1999
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
27
Review Days
14

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Basic Information

Device Name
GENZYME DIRECT AMYLASE VERIFIER
K Number
K993132
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genzyme Corp.
Date Received
September 20, 1999
Decision Date
October 4, 1999
Product Code
JIT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
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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