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

MISSION CONTROLS

K Number: K033063 · Decision Dec 12, 2003
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
66
Applicant Total
26
Review Days
74

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Basic Information

Device Name
MISSION CONTROLS
K Number
K033063
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diamond Diagnostics, Inc.
Date Received
September 29, 2003
Decision Date
December 12, 2003
Product Code
JJS
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
JJS Controls For Blood-Gases, (Assayed And Unassayed)

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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. →