INTRAOCULAR ELECTROMAGNET— 510(k) K854870

Substantially Equivalent

Mira, Inc.

FDA 510(k) clearance K854870 for INTRAOCULAR ELECTROMAGNET, Substantially Equivalent on 1986-02-19. Applicant: Mira, Inc.. Device class: 2.

Clearance details

Applicant: Mira, Inc.
Product code: Code HPO
Device class: Class 2
Regulation: 21 CFR 886.4440
Advisory panel: Ophthalmic
Date received: 1985-12-04
Decision date: 1986-02-19
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.