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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name airway, oropharyngeal, anesthesiology
510(k) Number K833482
Device Name WISDOM AIRWAY
Applicant
WISDOM CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
WISDOM CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5110
Classification Product Code
CAE  
Date Received10/07/1983
Decision Date 12/05/1983
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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