Medical Devices, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
49
Inspections
2
Compliance Actions
0

Known Names

medical devices, medical devices co

Recent 510(k) Clearances

K-NumberDeviceDate
K002280PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602February 5, 2001
K930084MICRO-ARTHROSCOPESeptember 1, 1995
K943126ELECTROFLEXDecember 5, 1994
K940012SMARTBRACE ELECTRODEDecember 5, 1994
K935132HOME MICROCURRENT HMCMarch 14, 1994
K934619FLEXMATEFebruary 23, 1994
K924897XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300July 6, 1993
K930053VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10May 17, 1993
K923914IF-II (TM), MODEL 7200November 6, 1992
K920071MEDITRON AUTOMATIC ELECTRONIC INSUFF. MODEL AEI-15July 21, 1992
K915694MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATORJune 18, 1992
K915408BIPOLAR ENDOSTASIS PROBE, BEST (TM)March 11, 1992
K912182MEDITRON COMBINATION GENERATOR CG-2000September 6, 1991
K912348SX90 (TM),MODEL 4800SJune 24, 1991
K905133STYLET TRACHAEL TUBEApril 22, 1991
K903161MC II (TM), MODEL 7200SMarch 27, 1991
K901302BIPOLARD POLYPECTOMY SYSTEM (TM)June 6, 1990
K895473DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700SDecember 8, 1989
K883462IF-II (TM), MODEL 9800May 24, 1989
K890705MEDIMOD(TM), MODEL 8900March 9, 1989