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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Administration, Intravascular
510(k) Number K905208
Device Name MORSE ANESTHESIA
Applicant
North American Instrument Corp.
Glens Falls,  NY  12801
Applicant Contact ROBERT FRANKLIN
Correspondent
North American Instrument Corp.
Glens Falls,  NY  12801
Correspondent Contact ROBERT FRANKLIN
Regulation Number880.5440
Classification Product Code
FPA  
Date Received11/20/1990
Decision Date 01/10/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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