# Olsen Electrosurgical, Inc.

- Location (FDA's records): Concord, CA
- FDA decisions: 11 (1988–1994): 11 510(k) clearances
- Product codes: HAM (5), GEI (4), FYD (1), HIB (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: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Misonix, Inc.: 1 (https://510kreport.com/company/misonix)
- Microline Pentax, Inc.: 1 (https://510kreport.com/company/microline-pentax)
- Itl Corporation Pty, Ltd.: 1 (https://510kreport.com/company/itl)

## Its most-cited devices
- K913108: Teflon Coated Electrodes/Electrodes Handles (1991), cited by 2
- K884172: Modified Olsen #770 Disposable Holster (1988), cited by 1

## Recent decisions
- K922154: Insulated Speculum W/ Smoke Evacuator Option (Apr 21, 1994)
- K912611: Olsen Laparoscopic Instr, Disposable, Single Use (Apr 15, 1992)
- K913108: Teflon Coated Electrodes/Electrodes Handles (Dec 23, 1991)
- K912612: Smoke/Odor Evacuator  #757 (Nov 1, 1991)
- K885199: #500 Series Forceps W/Cut/Coagulate Switches (Jan 13, 1989)
- K885200: 600 & 900 Series Electrodes & 755 & 756 Handle (Jan 13, 1989)
- K884171: #875 Disposable Biopolar Cable (Oct 24, 1988)
- K884174: Modified Olsen 755/756 Switchpens (Oct 24, 1988)

Source page: https://510kreport.com/company/olsen-electrosurgical