Marco Lm-770 Digital Projection Lensmeter

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

510(k) Number

K930445 ↗

FDA Product Code

HLM

Device Class

Class I

Regulation

21 CFR Part 886.1425

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Marco Gxx Series Photographic Slit Lamps

  Class II

  FDA 510(k) K930442 Active Cleared 9 Aug 1993

• Marco Surgiscope Operation Microscopes

  Class I

  FDA 510(k) K930439 Active Cleared 22 Jul 1993

• Marco Standard Radiusgauges

  Class I

  FDA 510(k) K930437 Active Cleared 9 Aug 1993

• Marco Projection Perimeter

  Class I

  FDA 510(k) K930448 Active Cleared 21 Jun 1993

• Ms-30 Automatic Perimeter

  Class I

  FDA 510(k) K943234 Active Cleared 27 Jul 1994

• Marco Standard Keratometers

  Class I

  FDA 510(k) K930444 Active Cleared 9 Aug 1993

See all devices from Marco Ophthalmic, Inc. →