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

AEROVENT

K Number: K894969 · Decision Oct 30, 1989
Classifications
1
FEI Numbers
167
Registration Numbers
167
Same Product Code
93
Applicant Total
33
Review Days
84

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Basic Information

Device Name
AEROVENT
K Number
K894969
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Monaghan Medical Corp.
Date Received
August 7, 1989
Decision Date
October 30, 1989
Product Code
BZA
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
BZA Connector, Airway (Extension)

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Other Clearances by Monaghan Medical Corp.

K Number Device Name
K123945 STRIVE DUAL ZONE PEAK FLOW METER
K031514 MODIFICATION TO TRUPEAK PEAK FLOW METER
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
Search all 33 clearances from Monaghan Medical Corp. →