LS1000 Surgical Aspirator II

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K854844 ↗

FDA Product Code

BTA

Device Class

Class II

Regulation

21 CFR Part 878.4780

Advisory Committee

General, Plastic Surgery

FDA Decision

SN

• LS9000 Suction Biopsy Needle

  Class I

  FDA 510(k) K862749 Active Cleared 15 Sep 1986

• LS3000 Cannula Uterine Suction

  Class II

  FDA 510(k) K862476 Active Cleared 18 Jul 1986

• Combo 36

  Class I

  FDA 510(k) K854257 Active Cleared 18 Nov 1985

• Modified Servo Syringe

  Class II

  FDA 510(k) K881521 Active Cleared 31 May 1988

• Auto Entry System (Mate)

  Class I

  FDA 510(k) K870425 Active Cleared 24 Mar 1987

• LM2000A Surgical Suction Monitor

  Class II

  FDA 510(k) K854359 Active Cleared 3 Mar 1986