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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Ventilator, Emergency, Powered (Resuscitator)
510(k) Number K924272
Device Name MEDIRESP III
Applicant
MEDFLOW CORP., INC.
100 HOGAN POINT RD.
HILTON,  NY  14468
Applicant Contact MURRAY E VOKES
Correspondent
MEDFLOW CORP., INC.
100 HOGAN POINT RD.
HILTON,  NY  14468
Correspondent Contact MURRAY E VOKES
Regulation Number868.5925
Classification Product Code
BTL  
Date Received08/24/1992
Decision Date 02/09/1994
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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