MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR— 510(k) K930449

Name: FDA 510(k) clearance K930449
Creator: U.S. Food and Drug Administration
Published: 1993-07-06

Substantially Equivalent

Marco Ophthalmic, Inc.

FDA 510(k) clearance K930449 for MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR, Substantially Equivalent on 1993-07-06. Applicant: Marco Ophthalmic, Inc.. Device class: 1.

Clearance details

Applicant: Marco Ophthalmic, Inc.
Product code: Code HME
Device class: Class 1
Regulation: 21 CFR 886.1140
Advisory panel: Ophthalmic
Date received: 1993-01-26
Decision date: 1993-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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