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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 K882930
Device Name LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX
Applicant
Pilling Co.
420 Delaware Dr.
Fort Washington,  PA  19034
Applicant Contact LELAND J WIMER
Correspondent
Pilling Co.
420 Delaware Dr.
Fort Washington,  PA  19034
Correspondent Contact LELAND J WIMER
Regulation Number868.5540
Classification Product Code
CCW  
Date Received07/13/1988
Decision Date 08/16/1988
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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