RICROKERATOME BLADE— 510(k) K992978

Substantially Equivalent

Surgistar, Inc.

FDA 510(k) clearance K992978 for RICROKERATOME BLADE, Substantially Equivalent on 1999-11-16. Applicant: Surgistar, Inc..

Clearance details

Applicant: Surgistar, Inc.
Product code: Code HNO
Advisory panel: Ophthalmic
Date received: 1999-09-03
Decision date: 1999-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, 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.