K100253

Substantially Equivalent

VISUMAX LASER KERATOME

Applicant: Carl Zeiss Meditec, AG
Product code: HQF
Advisory panel: Ophthalmic
Date received: 2010-01-28
Decision date: 2010-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, CA, US

Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

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.