One Incision Bi-Polar Electro. Forceps

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K781089 ↗

FDA Product Code

HIN

Device Class

Class II

Regulation

21 CFR Part 884.4150

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Forceps, Electrosurgical

  Class II

  FDA 510(k) K781109 Active Cleared 14 Sep 1978

• Insufflator, Model G100 & 200

  Class II

  FDA 510(k) K772297 Active Cleared 5 Jan 1978

• Laparoscopy Console Model VIII

  Class II

  FDA 510(k) K772242 Active Cleared 20 Dec 1977

• 8mm Trocar & Cannual W/Stopcock

  Class II

  FDA 510(k) K771964 Active Cleared 25 Oct 1977

• Scissors, Hook, Electrosurgical

  Class II

  FDA 510(k) K780954 Active Cleared 22 Jun 1978

• 12mm Self-Sealing Trocar & Cannula

  Class II

  FDA 510(k) K771958 Active Cleared 25 Oct 1977

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