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

DIAMOND CALIBRATOR LOW, DIAMOND CALIBRATOR HIGH

K Number: K121027 · Decision Dec 20, 2012
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
26
Review Days
260

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Basic Information

Device Name
DIAMOND CALIBRATOR LOW, DIAMOND CALIBRATOR HIGH
K Number
K121027
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diamond Diagnostics, Inc.
Date Received
April 4, 2012
Decision Date
December 20, 2012
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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K124009 MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS, LEVEL 1, MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS LEVEL 2, MISSION C
K121040 SMARTLYTE ELECTROLYTE ANALYZER
K121140 PROLYTE ELECTROLYTE ANALYZER
K120591 DIAMOND TOKYO BOEKI ISE MODULE CALIBRATOR 1,2,1-2
K103364 MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS, LEVEL 1, LEVEL 2, DUAL LEVEL
K102959 PROLYTE ELECTROLYTE ANALYZER
K093357 DIAMOND MEDICA ISE MODULE CALIBRANT A MODEL ME-6370D, DIAMOND MEDICA ISE MODULE CALIBRANT B, MODEL ME-5410D
K093492 MISSION CLINICHECK ASSAYED CHEMISTRY CONTROL, LEVEL 1&2, MISSION CLINICAL CALIBRATOR
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