# R. A. Fischer Co. Corp.

- Location (FDA's records): Glendale, CA
- FDA decisions: 13 (1976–1997): 13 510(k) clearances
- Product codes: KCW (8), IPF (2), EGJ (2), FTC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Selectivemed Components, Inc.: 1 (https://510kreport.com/company/selectivemed-components)
- Hidrex GmbH: 1 (https://510kreport.com/company/hidrex)
- Syneron Medical, Ltd.: 1 (https://510kreport.com/company/syneron-medical)

## Its most-cited devices
- K964208: MD-1A Galvanic Unit (1997), cited by 1
- K954031: Compu-Blend Epilator (1996), cited by 1
- K895365: MD-2 Iontophoresis Unit (1990), cited by 1

## Recent decisions
- K964208: MD-1A Galvanic Unit (Apr 30, 1997)
- K954031: Compu-Blend Epilator (Jan 5, 1996)
- K895365: MD-2 Iontophoresis Unit (Jun 26, 1990)
- K893389: Model SE-5 Epilator (Jun 5, 1989)
- K884079: Model CBX Epilator (Oct 4, 1988)
- K871372: CB-7 Electronic Epilator (Apr 28, 1987)
- K852534: Ultraviolet Treatment Lamps UV-8 & UV-9 (Nov 8, 1985)
- K843063: Electronic Epilator TS-1 (Sep 26, 1984)

Source page: https://510kreport.com/company/r-a-fischer