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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tube, tracheal (w/wo connector)
510(k) Number K023964
Device Name RUSCH MICROLARYNGEAL TUBE
Applicant
RUSCH INTL.
50 PLANTATION DR.
JAFFERY,  NH  03452
Applicant Contact RICK LYKINS
Correspondent
RUSCH INTL.
50 PLANTATION DR.
JAFFERY,  NH  03452
Correspondent Contact RICK LYKINS
Regulation Number868.5730
Classification Product Code
BTR  
Date Received11/29/2002
Decision Date 12/23/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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