Lm-100/200LOW Flow Insufflator

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K912789 ↗

FDA Product Code

HIG

Device Class

Class II

Regulation

21 CFR Part 884.1700

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• LM 1000 Cryosurgical Accessories

  Class II

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• Lm- Lap 10 High Flow Insufflator

  Class II

  FDA 510(k) K914201 Active Cleared 9 Jan 1992

• Colposcopes and Accessories

  Class II

  FDA 510(k) K940094 Active Cleared 25 Apr 1995

• Max-E-Vac

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  FDA 510(k) K920217 Active Cleared 23 Jul 1992

• Lm-1Z Zoom Scope

  Class II

  FDA 510(k) K902313 Active Cleared 4 Sep 1990

• LM-150HT Light Source

  Class III

  FDA 510(k) K911212 Active Cleared 23 May 1991

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