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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name regulator, pressure, gas cylinder
510(k) Number K862193
Device Name # 10099/10225/10235/10275/10525/10625/10715/10125
Applicant
U.O. EQUIPMENT CO.
P.O. BOX 500386
houston,  TX  77250
Applicant Contact wright
Correspondent
U.O. EQUIPMENT CO.
P.O. BOX 500386
houston,  TX  77250
Correspondent Contact wright
Regulation Number868.2700
Classification Product Code
CAN  
Date Received06/09/1986
Decision Date 07/09/1986
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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