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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stopcock, I.V. Set
510(k) Number K862691
Device Name STOPCOCK
Applicant
Ram Development
28 Remez St.
Nes-Ziona 70400
Israel,  IL
Applicant Contact ITZIK RABINOVITZ
Correspondent
Ram Development
28 Remez St.
Nes-Ziona 70400
Israel,  IL
Correspondent Contact ITZIK RABINOVITZ
Regulation Number880.5440
Classification Product Code
FMG  
Date Received07/15/1986
Decision Date 07/28/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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