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

22MM ID/OD ADAPTER

K Number: K911263 · Decision Aug 19, 1991
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
33
Review Days
150

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Basic Information

Device Name
22MM ID/OD ADAPTER
K Number
K911263
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5240
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Monaghan Medical Corp.
Date Received
March 22, 1991
Decision Date
August 19, 1991
Product Code
CAI
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
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)

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K123945 STRIVE DUAL ZONE PEAK FLOW METER
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K023097 TRUEZONE PEAK FLOW METER
K012939 AEROVENT II CHC COLLAPSIBLE HOLDING CHAMBER
K991212 MODIFICATION TO TRUZONE PEAK FLOW METER
K964130 AEROGEAR ASTHMA ACTION KIT
K963089 TRUZONE PEAK FLOW METER
K963095 TRUPEAK PEAK FLOW METER
K955234 TRUPEAK PEAK FLOW METER
K955262 TRUZONE PEAK FLOW METER
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