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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name nebulizer (direct patient interface)
510(k) Number K903580
Device Name MICRO-MISTER
Applicant
BP LTD.
P.O. BOX 3052
MIDDLETOWN,  NY  10940
Applicant Contact BORDONI
Correspondent
BP LTD.
P.O. BOX 3052
MIDDLETOWN,  NY  10940
Correspondent Contact BORDONI
Regulation Number868.5630
Classification Product Code
CAF  
Date Received08/08/1990
Decision Date 12/27/1990
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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