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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Filter, Intravascular, Cardiovascular
510(k) Number K870729
Device Name TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER
Applicant
MEDI-TECH, INC.
480 PLESANT ST.
P.O. BOX 7407
WATERTOWN,  MA  02272
Applicant Contact AL SEPRINSKI
Correspondent
MEDI-TECH, INC.
480 PLESANT ST.
P.O. BOX 7407
WATERTOWN,  MA  02272
Correspondent Contact AL SEPRINSKI
Regulation Number870.3375
Classification Product Code
DTK  
Date Received02/25/1987
Decision Date 04/09/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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