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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 K990547
Device Name PILLING WECK SURGICAL Y STENT FORCEPS
Applicant
PILLING WECK, INC.
1 WECK DR.
RESEARCH TRIANGLE PARK,  NC  27709
Applicant Contact JULIE A BEAUMONT
Correspondent
PILLING WECK, INC.
1 WECK DR.
RESEARCH TRIANGLE PARK,  NC  27709
Correspondent Contact JULIE A BEAUMONT
Regulation Number874.4680
Classification Product Code
EOQ  
Date Received02/22/1999
Decision Date 04/27/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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