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-Number | Device | Date |
|---|
| K110979 | DERMAGRIP ULTRA POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVES NON-STERILE,TESTED FOR USE W/ CH | October 20, 2011 |
| K000932 | ARACHNOPHLEBECTOMY NEEDLE | May 17, 2000 |
| K923995 | URODYNAMICS TUBING KITS #5161, #5150, #7170 | April 8, 1993 |
| K921426 | ULTRA PCI | October 5, 1992 |
| K912925 | ULTRA PVD | June 18, 1992 |
| K915658 | SPECTRA ECG | June 10, 1992 |
| K896103 | MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR | January 18, 1990 |
| K896102 | MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR | January 18, 1990 |
| K881905 | MODEL MICRO SI AMBULATORY ECG MONITOR | August 2, 1988 |
| K872508 | MODEL MICRO FD+ AMBULATORY ECG MONITOR | September 25, 1987 |
| K870538 | MODEL 192 PRINTER | April 23, 1987 |
| K870537 | MODEL MICRO ST AMBULATORY ECG MONITOR | April 23, 1987 |
| K852836 | ADVANCED MEDICAL PRODUCTS MINI-M (TENS) | August 28, 1985 |
| K852837 | ADVANCED MEDICAL PRODUCTS DR PULSE (TENS) | August 28, 1985 |
| K852838 | ADVANCED MEDICAL PRODUCTS MES TENS | August 28, 1985 |