Modified Servo Syringe

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K881521 ↗

FDA Product Code

DXT

Device Class

Class II

Regulation

21 CFR Part 870.1650

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• 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

• LS1000 Surgical Aspirator II

  Class II

  FDA 510(k) K854844 Active Cleared 12 Feb 1986

• Combo 36

  Class I

  FDA 510(k) K854257 Active Cleared 18 Nov 1985

• 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