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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name mask, oxygen
510(k) Number K962848
Device Name HANS RUDOLPH NASAL CPAP MASK
Applicant
HANS RUDOLPH, INC.
7200 WYANDOTTE
KANSAS CITY,  MO  64114
Applicant Contact KEVIN RUDOLPH
Correspondent
HANS RUDOLPH, INC.
7200 WYANDOTTE
KANSAS CITY,  MO  64114
Correspondent Contact KEVIN RUDOLPH
Regulation Number868.5580
Classification Product Code
BYG  
Date Received07/22/1996
Decision Date 10/16/1996
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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