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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name attachment, breathing, positive end expiratory pressure
510(k) Number K961867
Device Name PEEP VALVE
Applicant
MEDICAL MARKETING CONCEPTS
2310 YORK RD.
ROANOKE,  VA  24015
Applicant Contact BOB MARTIN
Correspondent
MEDICAL MARKETING CONCEPTS
2310 YORK RD.
ROANOKE,  VA  24015
Correspondent Contact BOB MARTIN
Regulation Number868.5965
Classification Product Code
BYE  
Date Received05/15/1996
Decision Date 08/13/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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