Reusable Laparoscopic Instruments W/ Electrocautery

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K930666 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Diamond-Touch and Micro Diamond-Touch Instruments/Diamond-Line Instruments/Diamond-Port(Access Parts)

  Class I

  FDA 510(k) K960400 Active Cleared 12 Mar 1996

• Endo I/a Y Set

  Class II

  FDA 510(k) K913979 Active Cleared 27 Nov 1991

• Electrosurgical Cutting and Coagulation Accessory

  Class II

  FDA 510(k) K861372 Active Cleared 19 Jun 1986

• Switchblade

  Class II

  FDA 510(k) K030890 Active Cleared 4 Apr 2003

• Snowden-Pencer Irrigation Pump

  Class II

  FDA 510(k) K920985 Active Cleared 9 Jun 1992

• Snowden-Pencer High Flow Insufflator, Sp/88-9700

  Class II

  FDA 510(k) K920986 Active Cleared 4 Jun 1992

See all devices from Snowden-Pencer →