Symbiosis Reusable Monopolar Electrosurgical Probe

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K941426 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Hot Biopsy Forceps

  Class II

  FDA 510(k) K910964 Active Cleared 2 May 1991

• Symbiosis Suction-Irrigator

  Class II

  FDA 510(k) K923563 Active Cleared 25 Nov 1992

• Symbiosis Disposable Urological Biopsy Forceps

  Class I

  FDA 510(k) K931957 Active Cleared 28 Feb 1994

• Turkel Thoracentesis System

  Class I

  FDA 510(k) K922614 Active Cleared 30 Jul 1992

• Symbiosis Gastrointestinal Biopsy Forceps

  Class I

  FDA 510(k) K946238 Active Cleared 20 Jan 1995

• Symbiosis Bipolar Forceps

  Class II

  FDA 510(k) K952432 Active Cleared 5 Jul 1995

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