# Advanced Medical Products, Inc.

- Location (FDA's records): Liverpool, NY
- FDA decisions: 14 (1985–2000): 14 510(k) clearances
- Product codes: GZJ (3), DSH (2), DSI (2), DXN (1), LOS (1), IYO (1), DSF (1), GAH (1), FAP (1), JAF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Pulse Biomedical, Inc.: 1 (https://510kreport.com/company/pulse-biomedical)
- Rozinn Electronics, Inc.: 1 (https://510kreport.com/company/rozinn-electronics)
- Venx, LLC: 1 (https://510kreport.com/company/venx)

## Its most-cited devices
- K881905: Model Micro SI Ambulatory Ecg Monitor (1988), cited by 2
- K000932: Arachnophlebectomy Needle (2000), cited by 1

## Recent decisions
- K000932: Arachnophlebectomy Needle (May 17, 2000)
- K923995: Urodynamics Tubing Kits #5161, #5150, #7170 (Apr 8, 1993)
- K921426: Ultra Pci (Oct 5, 1992)
- K912925: Ultra PVD (Jun 18, 1992)
- K915658: Spectra Ecg (Jun 10, 1992)
- K896102: Micro FD 7000 Ambulatory Blood Pressure Monitor (Jan 18, 1990)
- K896103: Micro FL 7400 Ambulatory Holter/BP Monitor (Jan 18, 1990)
- K881905: Model Micro SI Ambulatory Ecg Monitor (Aug 2, 1988)

Source page: https://510kreport.com/company/advanced-medical-products