MARCO PROJECTION PERIMETER— 510(k) K930448

Name: FDA 510(k) clearance K930448
Creator: U.S. Food and Drug Administration
Published: 1993-06-21

Substantially Equivalent

Marco Ophthalmic, Inc.

FDA 510(k) clearance K930448 for MARCO PROJECTION PERIMETER, Substantially Equivalent on 1993-06-21. Applicant: Marco Ophthalmic, Inc.. Device class: 1.

Clearance details

Applicant: Marco Ophthalmic, Inc.
Product code: Code HOO
Device class: Class 1
Regulation: 21 CFR 886.1605
Advisory panel: Ophthalmic
Date received: 1993-01-26
Decision date: 1993-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOO

view all

K941723 — WELCH ALLYN GLAUCOMA DETECTOR1994-06-06
K873912 — RICHMOND VISUAL FIELD SCREENER1987-11-02
K864467 — HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN1986-12-15
K860115 — DIGILAB CAMBRIDGE PERIMETER1986-02-27
K832800 — AUTOMATIC TANGENT SCREEN 501983-09-29

More clearances from Marco Ophthalmic, Inc.

view all

K943234 — MS-30 AUTOMATIC PERIMETER1994-07-27
K930437 — MARCO STANDARD RADIUSGAUGES1993-08-09
K930438 — MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPS1993-08-09
K930442 — MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPS1993-08-09
K930444 — MARCO STANDARD KERATOMETERS1993-08-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.