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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge
510(k) Number K863613
Device Name NO-FLO I
Applicant
Design Technologies, Inc.
1471 Pinewood St.
Rahway,  NJ  07065
Applicant Contact LOUIS G ACRI
Correspondent
Design Technologies, Inc.
1471 Pinewood St.
Rahway,  NJ  07065
Correspondent Contact LOUIS G ACRI
Regulation Number868.2300
Classification Product Code
CCN  
Date Received09/16/1986
Decision Date 12/15/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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