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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name connector, airway (extension)
510(k) Number K931345
Device Name CONNECTORS AND AIRWAY EXTENSIONS
Applicant
PRECISION MED PRODUCTS, LTD.
30 ROBB HILL RD.
SUITE B
MARRTINSVILLE,  IN  46151
Applicant Contact TIMOTHY STRUTHERS
Correspondent
PRECISION MED PRODUCTS, LTD.
30 ROBB HILL RD.
SUITE B
MARRTINSVILLE,  IN  46151
Correspondent Contact TIMOTHY STRUTHERS
Regulation Number868.5810
Classification Product Code
BZA  
Date Received03/17/1993
Decision Date 04/23/1993
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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