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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 K781213
Device Name COMPRESSOR, AIR, MINI-SILENT
Applicant
THE JOHN BUNN CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
THE JOHN BUNN CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.6250
Classification Product Code
BTI  
Date Received07/10/1978
Decision Date 07/27/1978
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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