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

AMYLASE REAGENT

K Number: K921057 · Decision Mar 27, 1992
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
98
Applicant Total
27
Review Days
22

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Basic Information

Device Name
AMYLASE REAGENT
K Number
K921057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1070
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Genzyme Corp.
Date Received
March 5, 1992
Decision Date
March 27, 1992
Product Code
JFJ
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
JFJ Catalytic Methods, Amylase

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K033864 GENZYME OSOM TRICHOMONAS RAPID TEST
K023544 GENZYME CONTRAST II HCG URINE/SERUM TEST
K021316 ULTRA N-GENEOUS HDL CHOLESTEROL REAGENT 1/REAGENT2; ULTRA N-GENEOUS HDL CHOLESTREOL CALIBRATOR
K021019 COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTURE
K012532 SEPRAGEL SINUS
K011843 GENZYME DIRECT-AMYLASE TEST REAGENT
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