FDA applicant
Advanced Medical Products, Inc.
FDA records 14 decisions for Advanced Medical Products, Inc. (Liverpool, NY) from 1985 to 2000: 14 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and DSH (Recorder, Magnetic Tape, Medical). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Advanced Medical Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Advanced Medical Products, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Advanced Medical Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report