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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Light Source, Fiberoptic, Routine
510(k) Number K771739
Device Name PENTAX LH-150F LIGHT SOURCE
Applicant
PILLING CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
PILLING CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.1500
Classification Product Code
FCW  
Date Received09/15/1977
Decision Date 09/30/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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