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Medical Device Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
46
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K101832BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENTAugust 27, 2010
K053518INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHORJanuary 26, 2006
K051421INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHORAugust 30, 2005
K050873CANALIZER HYDROPHILIC GUIDE WIREMay 26, 2005
K043523INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLEFebruary 11, 2005
K042464V-CORE FULL CORE BREAST BIOPSY INSTRUMENTSeptember 30, 2004
K040427FIBREX CATHETER PATENCY DEVICEMay 3, 2004
K031442PBN GUIDEWIRESAugust 13, 2003
K021606EN-SNARE ENDOVASCULAR SNARE AND CATHETERMay 31, 2002
K011790MICROCRUISER PLUS INTRODUCER SETSeptember 5, 2001
K000620PBN FALLOPIAN TUBE CATHETER SYSTEMOctober 30, 2000
K002416GOLDEN-RULE SCALING CATHETERSeptember 11, 2000
K000433PBN HYSTERO-SALPINGOGRAPHY CATHETER SETJune 16, 2000
K990808PBN DILATORSNovember 26, 1999
K990839TRU-CORE I REUSABLE BIOPSY INSTRUMENTMay 20, 1999
K991097PBN DRAINAGE CATHETER GUIDEWIRESApril 23, 1999
K982960MEICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSABLE AUTOMATIC BIOPSY INSTRUMENTSeptember 23, 1998
K982085MEDICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSALE SEMI-AUTOMATIC BIOPDY INSTRUMENTJuly 17, 1998
K980192MANAN NEPHROSTOMY DRAINAGE CATHETERMay 27, 1998
K980193MANAN GENERAL UTILITY DRAINAGE CATHETERMay 27, 1998