A&E Medical Electrosurgical Connecting Cords

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

510(k) Number

K930528 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Myo/Clip

  Class II

  FDA 510(k) K821518 Active Cleared 8 Jul 1982

• Electro-Cautery Suction Tube

  Class II

  FDA 510(k) K881413 Active Cleared 21 Apr 1988

• A&E Medical Corp Dispos Suct Coag W/Non Stick Coat

  Class II

  FDA 510(k) K914193 Active Cleared 5 Oct 1992

• A&E Medical Electrosurg Electro W/Non-Stick Coat

  Class II

  FDA 510(k) K931537 Active Cleared 7 Sep 1993

• A & E Medical Electrocautery Suction Tube with Finger Tip Activator Button

  Class II

  FDA 510(k) K964621 Active Cleared 20 Dec 1996

• Labeling for Myo/Wire II Sternotomy Sutures

  Class II

  FDA 510(k) K932513 Active Cleared 7 Jan 1994

See all devices from Alto Development Corp. →