510(k) Report

FDA applicant

Fisher Imaging Corp.

Reading, PA3 decisions1986–19950 recalls

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, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

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.

FIG. 1 — Fisher Imaging Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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Other applicant names beginning “Fisher”

FDA records each applicant name separately; these may or may not be the same firm.