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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name tubing, pressure and accessories
510(k) Number K853569
Device Name MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING
Applicant
MEDIPART JERRY ALEXANDER
607 SPRING BEACH RD.
CARY,  IL  60013
Applicant Contact JERRY ALEXANDER
Correspondent
MEDIPART JERRY ALEXANDER
607 SPRING BEACH RD.
CARY,  IL  60013
Correspondent Contact JERRY ALEXANDER
Regulation Number868.5860
Classification Product Code
BYX  
Date Received08/26/1985
Decision Date 11/07/1985
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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