Marco Ophthalmic, Inc.
Marco Ophthalmic, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1994.
Top product codes for Marco Ophthalmic, Inc.
Recent clearances by Marco Ophthalmic, Inc.
- K943234 — MS-30 AUTOMATIC PERIMETER
- K930437 — MARCO STANDARD RADIUSGAUGES
- K930438 — MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPS
- K930442 — MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPS
- K930444 — MARCO STANDARD KERATOMETERS
- K930439 — MARCO SURGISCOPE OPERATION MICROSCOPES
- K930440 — MARCO INTERNATIONAL STAND
- K930441 — MARCO STANDARD LENSMETERS 101,201
- K930443 — MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJE
- K930446 — MARCO TRIAL SETS
- K930447 — MARCO H AND TS-1 INSTRUMENT TABLES
- K930449 — MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR
- K930445 — MARCO LM-770 DIGITAL PROJECTION LENSMETER
- K930448 — MARCO PROJECTION PERIMETER
- K921320 — ELIOS DIODE OPHTHALMIC LASER
Data sourced from openFDA. This site is unofficial and independent of the FDA.