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Marco Ophthalmic, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943234MS-30 AUTOMATIC PERIMETERJuly 27, 1994
K930444MARCO STANDARD KERATOMETERSAugust 9, 1993
K930442MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPSAugust 9, 1993
K930437MARCO STANDARD RADIUSGAUGESAugust 9, 1993
K930438MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPSAugust 9, 1993
K930439MARCO SURGISCOPE OPERATION MICROSCOPESJuly 22, 1993
K930440MARCO INTERNATIONAL STANDJuly 6, 1993
K930447MARCO H AND TS-1 INSTRUMENT TABLESJuly 6, 1993
K930449MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIRJuly 6, 1993
K930443MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJEJuly 6, 1993
K930441MARCO STANDARD LENSMETERS 101,201July 6, 1993
K930446MARCO TRIAL SETSJuly 6, 1993
K930445MARCO LM-770 DIGITAL PROJECTION LENSMETERJune 21, 1993
K930448MARCO PROJECTION PERIMETERJune 21, 1993
K921320ELIOS DIODE OPHTHALMIC LASERJuly 2, 1992