FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

P-AMYLASE CONTROL

K Number: K935362 · Decision Jan 27, 1994
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
6
Review Days
84

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Basic Information

Device Name
P-AMYLASE CONTROL
K Number
K935362
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman
Date Received
November 4, 1993
Decision Date
January 27, 1994
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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Other Clearances by Beckman

K Number Device Name
K991707 MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206
K971534 SYNCHRON SYUSTEMS DAT DRUG FREE URINE CONTROL
K904219 SYNCHRON CX 7 CLINICAL ANALYZER
K904220 SYNCHRON CX4-CE
K893583 BECKMAN CHOLINESTERASE REAGENT KIT