FDA applicant
R. A. Fischer Co. Corp.
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
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.
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.
See the 510(k) Report