Marco Ophthalmic, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marco Ophthalmic, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Marco Ophthalmic, Inc. has 15 FDA 510(k) cleared ophthalmic devices. Based in Jacksonville, US.
Historical record: 15 cleared submissions from 1992 to 1994.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Marco Ophthalmic, Inc.
15 devices
Cleared
Jul 27, 1994
MS-30 AUTOMATIC PERIMETER
Ophthalmic
21d
Cleared
Aug 09, 1993
MARCO STANDARD RADIUSGAUGES
Ophthalmic
195d
Cleared
Aug 09, 1993
MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPS
Ophthalmic
195d
Cleared
Aug 09, 1993
MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPS
Ophthalmic
195d
Cleared
Aug 09, 1993
MARCO STANDARD KERATOMETERS
Ophthalmic
195d
Cleared
Jul 22, 1993
MARCO SURGISCOPE OPERATION MICROSCOPES
General & Plastic Surgery
177d
Cleared
Jul 06, 1993
MARCO INTERNATIONAL STAND
Ophthalmic
161d
Cleared
Jul 06, 1993
MARCO STANDARD LENSMETERS 101,201
Ophthalmic
161d
Cleared
Jul 06, 1993
MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJE
Ophthalmic
161d
Cleared
Jul 06, 1993
MARCO TRIAL SETS
Ophthalmic
161d
Cleared
Jul 06, 1993
MARCO H AND TS-1 INSTRUMENT TABLES
Ophthalmic
161d
Cleared
Jul 06, 1993
MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR
Ophthalmic
161d