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

MOUTH TO MASK EMERGENCY VENTILATION

K Number: K841429 · Decision Apr 17, 1984
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
56
Applicant Total
14
Review Days
11

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Basic Information

Device Name
MOUTH TO MASK EMERGENCY VENTILATION
K Number
K841429
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5110
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
O-Two Systems Intl., Inc.
Date Received
April 6, 1984
Decision Date
April 17, 1984
Product Code
CAE
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
CAE Airway, Oropharyngeal, Anesthesiology

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Other Clearances by O-Two Systems Intl., Inc.

K Number Device Name
K991195 CAREVENT BLS, CAREVENT BLS+, CAREVENT ALS, CAREVENT ALS+, AND CAREVENT ATV
K983857 AUTOVENT 1500
K983785 AUTOVENT 1000
K983643 GENESIS BLS
K983705 EMT RESUSCITATOR
K960995 CPR BIO-BARRIER FACESHEILD
K940712 PPM III
K940927 RESCUE BREATHER
K932170 FLYNNR GENESIS II A/C, A/O AND IDLH
K922810 ODYSSEY
Search all 14 clearances from O-Two Systems Intl., Inc. →