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

OXYGEN CONCENTRATION INDICATOR

K Number: K944654 · Decision Nov 8, 1994
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
24
Review Days
48

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Basic Information

Device Name
OXYGEN CONCENTRATION INDICATOR
K Number
K944654
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Aequitron Medical, Inc.
Date Received
September 21, 1994
Decision Date
November 8, 1994
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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Other Clearances by Aequitron Medical, Inc.

K Number Device Name
K961972 MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR
K952880 MODEL LP-1000 VOLUME VENTILATOR
K914424 MODEL 6213 REMOTE ALARM
K915381 PORTABLE OXYGEN GENERATOR
K911399 NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)
K903020 RESPIRATION/HEART RATE MONITOR MODEL 9500/9550
K905244 MODEL LP6 VENTILATOR, MODIFICATION
K903010 CONTINUOUS VOLUME VENTILATOR MODEL LP10
K902785 MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON
K901656 MODEL 9200 RESPIRATION/HEART RATE MONITOR
Search all 24 clearances from Aequitron Medical, Inc. →