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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Generator, Oxygen, Portable
510(k) Number K873156
Device Name AMOX OXYGEN GENERATORS
Applicant
VBM CORP.
POST OFFICE BOX 922
LOUISVILLE,  KY  40201
Applicant Contact JOHN DORWART
Correspondent
VBM CORP.
POST OFFICE BOX 922
LOUISVILLE,  KY  40201
Correspondent Contact JOHN DORWART
Regulation Number868.5440
Classification Product Code
CAW  
Date Received07/31/1987
Decision Date 01/22/1988
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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