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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Support, Patient Position
510(k) Number K934235
Device Name SNIFF POSITION PILLOW
Applicant
AMERICAN MEDICAL DEVELOPMENT, INC.
220 COMMERCIAL ST.
BOSTON,  MA  02109
Applicant Contact MARK VANDER WERF
Correspondent
AMERICAN MEDICAL DEVELOPMENT, INC.
220 COMMERCIAL ST.
BOSTON,  MA  02109
Correspondent Contact MARK VANDER WERF
Regulation Number868.6820
Classification Product Code
CCX  
Date Received08/30/1993
Decision Date 10/01/1993
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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