CONVERTER SYSTEM— 510(k) K894248

Substantially Equivalent

Mira, Inc.

FDA 510(k) clearance K894248 for CONVERTER SYSTEM, Substantially Equivalent on 1990-02-27. Applicant: Mira, Inc..

Clearance details

Applicant: Mira, Inc.
Product code: Code HQE
Advisory panel: Ophthalmic
Date received: 1989-06-21
Decision date: 1990-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

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Adverse events under product code HQE

product code HQE

Injury: 156
Malfunction: 565
Total: 721

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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