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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laryngoscope, Rigid
510(k) Number K915804
Device Name PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.
Applicant
Propper Mfg. Co., Inc.
3604 Skillman Ave.
Long Island City,  NY  11101
Applicant Contact KENNETH SUMMER
Correspondent
Propper Mfg. Co., Inc.
3604 Skillman Ave.
Long Island City,  NY  11101
Correspondent Contact KENNETH SUMMER
Regulation Number868.5540
Classification Product Code
CCW  
Date Received12/24/1991
Decision Date 03/20/1992
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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