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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Airway, Oropharyngeal, Anesthesiology
510(k) Number K855137
Device Name CURITY FIBEROPTIC INTUBATING AIRWAY
Applicant
The Kendal Co.
One Federal St.
Boston,  MA  02110
Applicant Contact MARK W WENZEL
Correspondent
The Kendal Co.
One Federal St.
Boston,  MA  02110
Correspondent Contact MARK W WENZEL
Regulation Number868.5110
Classification Product Code
CAE  
Date Received12/23/1985
Decision Date 03/11/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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