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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 K871829
Device Name SIEMENS DRY AIR COMPRESSOR
Applicant
SIEMENS ELEMA AB
2360 NORTH PALMER DR.
P.O. BOX 94517
SCHAUMBURG,  IL  60195
Applicant Contact ELLEN FARNEY
Correspondent
SIEMENS ELEMA AB
2360 NORTH PALMER DR.
P.O. BOX 94517
SCHAUMBURG,  IL  60195
Correspondent Contact ELLEN FARNEY
Regulation Number868.6250
Classification Product Code
BTI  
Date Received05/11/1987
Decision Date 06/15/1987
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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