FDA applicant
Fisher Imaging Corp.
FDA records 3 decisions for Fisher Imaging Corp. (Reading, PA) from 1986 to 1995: 3 510(k) clearances. Most are in product codes DRR (Amplifier And Signal Conditioner, Biopotential) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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 Fisher Imaging Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Fisher Imaging Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Fisher Imaging Corp.’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) ReportOther applicant names beginning “Fisher”
FDA records each applicant name separately; these may or may not be the same firm.