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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 K140049
Device Name MOVES SLC
Applicant
THORNHILL RESEARCH INC
210 DUNDAS STREET WEST
TORONTO,  CA M5G2E8
Applicant Contact CLIFF ANSEL
Correspondent
THORNHILL RESEARCH INC
210 DUNDAS STREET WEST
TORONTO,  CA M5G2E8
Correspondent Contact CLIFF ANSEL
Regulation Number868.5925
Classification Product Code
BTL  
Date Received01/09/2014
Decision Date 05/29/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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