VISTITOME 20-10 MICROKERATOME— 510(k) K014000

Substantially Equivalent

Biovision AG

FDA 510(k) clearance K014000 for VISTITOME 20-10 MICROKERATOME, Substantially Equivalent on 2002-03-11. Applicant: Biovision AG.

Clearance details

Applicant: Biovision AG
Product code: Code HNO
Advisory panel: Ophthalmic
Date received: 2001-12-04
Decision date: 2002-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code HNO

product code HNO

Injury: 390
Total: 390

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.