Jacobs High Vacuum Suction Unit 05-2570

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K843693 ↗

FDA Product Code

BTA

Device Class

Class II

Regulation

21 CFR Part 878.4780

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Kogan Endospeculum 9-1/2

  Class I

  FDA 510(k) K842111 Active Cleared 19 Jun 1984

• Rudd-Clinic Hemorrhoidal Forceps

  Class I

  FDA 510(k) K800441 Active Cleared 8 Apr 1980

• Miniclamps, Stabiliz., Fallopian Tube Open recall

  Class II

  FDA 510(k) K772229 Active Cleared 3 Jan 1978

• Gusberg Hysterectomy Clamp

  Class I

  FDA 510(k) K771344 Active Cleared 27 Jul 1977

• Hemorrhoidal Ligator

  Class I

  FDA 510(k) K790577 Active Cleared 23 Apr 1979

• Leff Stethoscope for Fetal Heart

  Class I

  FDA 510(k) K761338 Active Cleared 12 Jan 1977

See all devices from J. Sklar Mfg. Co., Inc. →