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

CALIBRATING MATERIAL,CAL-PAK, CAL & SLOPE STANDARDS

K Number: K020596 · Decision Mar 23, 2002
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
26
Review Days
29

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Basic Information

Device Name
CALIBRATING MATERIAL,CAL-PAK, CAL & SLOPE STANDARDS
K Number
K020596
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
February 22, 2002
Decision Date
March 23, 2002
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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Other Clearances by Diamond Diagnostics, Inc.

K Number Device Name
K200544 SmartLyte® Plus Electrolyte Analyzer Na+/K+/Cl-/Ca++/Li+
K133751 DIAMOND DIAGNOSTICS ISE SERUM STANDARDS, DIAMOND DIAGNOSTICS ISE URINE STANDARDS
K124009 MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS, LEVEL 1, MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS LEVEL 2, MISSION C
K121027 DIAMOND CALIBRATOR LOW, DIAMOND CALIBRATOR HIGH
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
Search all 26 clearances from Diamond Diagnostics, Inc. →