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

OXYGEN ANALYZER, MODELS AII 20000A, AII 2000HC, AII 2000M

K Number: K053407 · Decision Apr 5, 2006
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
3
Review Days
119

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Basic Information

Device Name
OXYGEN ANALYZER, MODELS AII 20000A, AII 2000HC, AII 2000M
K Number
K053407
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Analytical Industries, Inc.
Date Received
December 7, 2005
Decision Date
April 5, 2006
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CCL), ordered by most recent decision date.

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Other Clearances by Analytical Industries, Inc.

K Number Device Name
K002382 'ALL 2000' % OXYGEN ANALYZER
K952736 PERCENT OXYGEN SENSOR