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

ELECTROPHORESIS CONTROL LEVEL 1

K Number: K925326 · Decision Mar 26, 1993
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
28
Review Days
156

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Basic Information

Device Name
ELECTROPHORESIS CONTROL LEVEL 1
K Number
K925326
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Seradyn, Inc.
Date Received
October 21, 1992
Decision Date
March 26, 1993
Product Code
JJY
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

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K062204 ARCHITECT CORTISOL ASSAY
K060998 QMS TOBRAMYCIN
K060709 MULTIGENT GENTAMICIN
K052826 QMS QUINIDINE. QMS QUINIDINE CALIBRATORS
K051211 QMS ZONISAMIDE REAGENTS, CALIBRATORS AND CONTROLS
K052815 QMS AMIKACIN REAGENTS
K050419 QMS VANCOMYCIN
K042307 ARCHITECT T-UPTAKE CALIBRATORS (A-F) AND CONTROLS (LOW, HIGH)
Search all 28 clearances from Seradyn, Inc. →