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Medical Dynamics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K974542TRUE VISION, TRUE VISION IIFebruary 17, 1998
K921294VIDEO ENDOSCOPE-RIGID MODIFICATIONJuly 20, 1994
K934682SURGICAL VIDEO CAMERA AND ACCESSORIESFebruary 15, 1994
K930568ADAIR/VERESS NEEDLE INTRODUCER SETJuly 22, 1993
K915538OVER THE WIRE STONE BASKETMarch 20, 1992
K914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATIONMarch 4, 1992
K913986CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEMJanuary 28, 1992
K911296OPTICAL CATHETER ARTHROSCOPESeptember 24, 1991
K903339VIDEO ENDOSCOPE, RIGIDMarch 6, 1991
K904609XENON LIGHT SOURCEDecember 18, 1990
K904113OPERATIVE RECORDING CAMERAOctober 30, 1990
K900374ADAIR/VERESS NEEDLE INTRODUCER SETApril 20, 1990
K896008MODEL 6500 MERCURY ARC LIGHT SOURCEDecember 27, 1989
K895041OPTICAL CATHETER(TM) INTRODUCER SETSOctober 16, 1989
K894319MEDICAL DYNAMICS LIGHT SOURCEOctober 3, 1989
K891983CAM-WRAP(TM) NEW STERILIZATION PROCEDUREApril 19, 1989
K891236FDX SOLID STATE VIDEO CAMERA MODEL 5950April 5, 1989
K884039MEDICAL DYNAMICS SOLID STATE VIDEO CAMERA 5940October 13, 1988