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

DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE (MODEL FAMILY E-CAIOVX) E-CAIOVX, E-CAIOV, E-CAIO, E-COVX, E-COV, E-CO & ACCESACC

K Number: K051092 · Decision May 25, 2005
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
168
Review Days
27

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Basic Information

Device Name
DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE (MODEL FAMILY E-CAIOVX) E-CAIOVX, E-CAIOV, E-CAIO, E-COVX, E-COV, E-CO & ACCESACC
K Number
K051092
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
April 28, 2005
Decision Date
May 25, 2005
Product Code
CCL
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

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