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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 K820079
Device Name AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL
Applicant
JAMES L. GERACI & ASSOCIATES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
JAMES L. GERACI & ASSOCIATES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.6250
Classification Product Code
BTI  
Date Received01/12/1982
Decision Date 02/05/1982
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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