Advanced Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K110979DERMAGRIP ULTRA POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVES NON-STERILE,TESTED FOR USE W/ CHOctober 20, 2011
K000932ARACHNOPHLEBECTOMY NEEDLEMay 17, 2000
K923995URODYNAMICS TUBING KITS #5161, #5150, #7170April 8, 1993
K921426ULTRA PCIOctober 5, 1992
K912925ULTRA PVDJune 18, 1992
K915658SPECTRA ECGJune 10, 1992
K896103MICRO FL 7400 AMBULATORY HOLTER/BP MONITORJanuary 18, 1990
K896102MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITORJanuary 18, 1990
K881905MODEL MICRO SI AMBULATORY ECG MONITORAugust 2, 1988
K872508MODEL MICRO FD+ AMBULATORY ECG MONITORSeptember 25, 1987
K870537MODEL MICRO ST AMBULATORY ECG MONITORApril 23, 1987
K870538MODEL 192 PRINTERApril 23, 1987
K852838ADVANCED MEDICAL PRODUCTS MES TENSAugust 28, 1985
K852837ADVANCED MEDICAL PRODUCTS DR PULSE (TENS)August 28, 1985
K852836ADVANCED MEDICAL PRODUCTS MINI-M (TENS)August 28, 1985