MARCO STANDARD RADIUSGAUGES— 510(k) K930437

Name: FDA 510(k) clearance K930437
Creator: U.S. Food and Drug Administration
Published: 1993-08-09

Substantially Equivalent

Marco Ophthalmic, Inc.

FDA 510(k) clearance K930437 for MARCO STANDARD RADIUSGAUGES, Substantially Equivalent on 1993-08-09. Applicant: Marco Ophthalmic, Inc.. Device class: 1.

Clearance details

Applicant: Marco Ophthalmic, Inc.
Product code: Code HLF
Device class: Class 1
Regulation: 21 CFR 886.1430
Advisory panel: Ophthalmic
Date received: 1993-01-26
Decision date: 1993-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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