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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Bronchoscope (Flexible Or Rigid)
510(k) Number K760171
Device Name FIBERBRONCHOSCOPE (PENTAX FB-17A)
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 Number874.4680
Classification Product Code
EOQ  
Date Received07/06/1976
Decision Date 07/19/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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