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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name compressor, air, portable
510(k) Number K832220
Device Name TRAVELER NEBULIZING SYSTEM
Applicant
MEDIX OF FLORIDA, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
MEDIX OF FLORIDA, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.6250
Classification Product Code
BTI  
Date Received07/08/1983
Decision Date 09/26/1983
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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