INTRAOCULAR PRESSURE REDUCER— 510(k) K854873

Substantially Equivalent

Mira, Inc.

FDA 510(k) clearance K854873 for INTRAOCULAR PRESSURE REDUCER, Substantially Equivalent on 1986-02-04. Applicant: Mira, Inc.. Device class: 2.

Clearance details

Applicant: Mira, Inc.
Product code: Code LCR
Device class: Class 2
Regulation: 21 CFR 862.3900
Advisory panel: Clinical Toxicology
Date received: 1985-12-04
Decision date: 1986-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

Download summary PDF View on FDA.gov ↗

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