Advanced Medical Products, Inc.
Clarksville, MD, US
Advanced Medical Products, Inc. appears in FDA device records in Clarksville, MD. FDA records list 14 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Advanced Medical Products, Inc. between 1985 and 2000. The busiest year on record is 1985, with 3. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 3 |
| 1987 | 3 |
| 1988 | 1 |
| 1990 | 2 |
| 1992 | 3 |
| 1993 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K000932 | ARACHNOPHLEBECTOMY NEEDLE | GAH | Substantially Equivalent | |
| K923995 | URODYNAMICS TUBING KITS #5161, #5150, #7170 | FAP | Substantially Equivalent | |
| K921426 | ULTRA PCI | IYO | Substantially Equivalent | |
| K912925 | ULTRA PVD | JAF | Substantially Equivalent | |
| K915658 | SPECTRA ECG | LOS | Substantially Equivalent | |
| K896103 | MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR | DSI | Substantially Equivalent | |
| K896102 | MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | |
| K881905 | MODEL MICRO SI AMBULATORY ECG MONITOR | DSI | Substantially Equivalent | |
| K872508 | MODEL MICRO FD+ AMBULATORY ECG MONITOR | DSH | Substantially Equivalent | |
| K870538 | MODEL 192 PRINTER | DSF | Substantially Equivalent | |
| K870537 | MODEL MICRO ST AMBULATORY ECG MONITOR | DSH | Substantially Equivalent | |
| K852838 | ADVANCED MEDICAL PRODUCTS MES TENS | GZJ | Substantially Equivalent | |
| K852837 | ADVANCED MEDICAL PRODUCTS DR PULSE (TENS) | GZJ | Substantially Equivalent | |
| K852836 | ADVANCED MEDICAL PRODUCTS MINI-M (TENS) | GZJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- FAPCystometric Gas (Carbon-Dioxide) On Hydraulic Device
- DSIDetector And Alarm, Arrhythmia
- JAFMonitor, Ultrasonic, Nonfetal
- DSHRecorder, Magnetic Tape, Medical
- DSFRecorder, Paper Chart
- GZJStimulator, Nerve, Transcutaneous, For Pain Relief
- GAHStylet, Surgical, General & Plastic Surgery
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- DXNSystem, Measurement, Blood-Pressure, Non-Invasive
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain