FDA 510(k) Application Details - K000229

Device Classification Name Light Source, Fiberoptic, Routine

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510(K) Number K000229
Device Name Light Source, Fiberoptic, Routine
Applicant VIDEOLABS, INC.
2530 PENNSYLVANIA AVE.
SAINT LOUIS PARK, MN 55426 US
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Contact FRANK B FREEDMAN
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Regulation Number 876.1500

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Classification Product Code FCW
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Date Received 01/27/2000
Decision Date 03/21/2000
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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