510(k) Report

FDA applicant

R. A. Fischer Co. Corp.

Glendale, CA13 decisions1976–19970 recalls

FDA records 13 decisions for R. A. Fischer Co. Corp. (Glendale, CA) from 1976 to 1997: 13 510(k) clearances. Most are in product codes KCW (Epilator, High Frequency, Needle-Type) and IPF (Stimulator, Muscle, Powered). 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, general and plastic surgery panel, where it files most

How often FDA has decided R. A. Fischer Co. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for R. A. Fischer Co. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like R. A. Fischer Co. 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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