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

ELECTROPHORESIS CONTROL

K Number: K910160 · Decision Feb 27, 1991
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
28
Review Days
43

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Basic Information

Device Name
ELECTROPHORESIS CONTROL
K Number
K910160
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Seradyn, Inc.
Date Received
January 15, 1991
Decision Date
February 27, 1991
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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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)
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