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

BLOOD GASES/PC02, PO2 ANALYSIS PRODUCTS

K Number: K902267 · Decision Jun 12, 1990
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
21
Review Days
22

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Basic Information

Device Name
BLOOD GASES/PC02, PO2 ANALYSIS PRODUCTS
K Number
K902267
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Phoenix Diagnostics, Inc.
Date Received
May 21, 1990
Decision Date
June 12, 1990
Product Code
CHL
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
CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

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Other Clearances by Phoenix Diagnostics, Inc.

K Number Device Name
K023268 PHOENIX ISE STANDARD A,B AND C FOR ROCHE/AVL SYSTEMS
K020364 PHOENIX ISE REAGENTS FOR BECKMAN CX SYSTEMS
K020148 pHoenix ISE Reagents FOR Olympus AU Chemistry Systems
K020129 PHOENIX ELETROLYTE CALIBRATION SET FOR THE ROCHE COBAS ISE MODULE
K013451 PHOENOIX ISE REAGENTS FOR ROCHE HITACHI, MODELS 700/900 SERIES
K012987 PHOENIX ELECTROLYTE CALIBRATION SET FOR THE MEDICAL EASYLYTE CALCIUM ANALYZER
K012509 PHOENIX ELECTROLYTE CALIBRATION SET FOR THE DADE/BEHRING/BEHRING DIMENSION CHEMISTRY SYSTEM
K960592 ELECTROLYTE STANDARDS
K945860 SPECTRUM CO-OXIMETER LINEARITY CONTROL
K920285 BLOOD GAS/ISE LINEARITY CONTROL
Search all 21 clearances from Phoenix Diagnostics, Inc. →