Modified Olsen #770 Disposable Holster

No FDA recalls found in the data synced 6 Oct 2026.

510(k) Number

K884172 ↗

FDA Product Code

HAM

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• #820/821 Bipolar Forceps

  Class II

  FDA 510(k) K884175 Active Cleared 24 Oct 1988

• 600 & 900 Series Electrodes & 755 & 756 Handle

  Class II

  FDA 510(k) K885200 Active Cleared 13 Jan 1989

• Insulated Speculum W/ Smoke Evacuator Option

  Class II

  FDA 510(k) K922154 Active Cleared 21 Apr 1994

• #500 Series Forceps W/Cut/Coagulate Switches

  Class II

  FDA 510(k) K885199 Active Cleared 13 Jan 1989

• Olsen Laparoscopic Instr, Disposable, Single Use

  Class II

  FDA 510(k) K912611 Active Cleared 15 Apr 1992

• Teflon Coated Electrodes/Electrodes Handles

  Class II

  FDA 510(k) K913108 Active Cleared 23 Dec 1991

See all devices from Olsen Electrosurgical, Inc. →

• What is the Modified Olsen #770 Disposable Holster used for?

  The Modified Olsen #770 Disposable Holster is a manual surgical instrument designed for general use in various general and plastic surgery procedures. It is a nonpowered, hand-held device that assists surgeons during surgical interventions.

• Is the Modified Olsen #770 Disposable Holster single-use or reusable?

  The Modified Olsen #770 Disposable Holster is designed as a disposable device, meaning it is intended for single-use only. After use, it should be properly disposed of according to medical waste protocols.

• What are the storage requirements for the Modified Olsen #770 Disposable Holster?

  The Modified Olsen #770 Disposable Holster is stored at the manufacturer's facility in Concord, California. It should be kept in a clean, dry environment until use to maintain its integrity and functionality.

• What regulatory approvals does the Modified Olsen #770 Disposable Holster have?

  The Modified Olsen #770 Disposable Holster has FDA 510(k) clearance with product code HAM and is classified for use in General and Plastic Surgery. It was cleared on October 24, 1988, with the K number K884172.