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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name monitor, airway pressure (includes gauge and/or alarm)
510(k) Number K940375
Device Name MICRO MPM
Applicant
MICRO DIRECT, INC.
120 CENTER ST. #105
AUBURN,  ME  04210
Applicant Contact DAVID R STASZAK
Correspondent
MICRO DIRECT, INC.
120 CENTER ST. #105
AUBURN,  ME  04210
Correspondent Contact DAVID R STASZAK
Regulation Number868.2600
Classification Product Code
CAP  
Date Received01/26/1994
Decision Date 11/21/1994
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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