ELECTRO-KERATOTOME, LINE-OPERATED— 510(k) K760726

Substantially Equivalent

Storz Instrument Co.

FDA 510(k) clearance K760726 for ELECTRO-KERATOTOME, LINE-OPERATED, Substantially Equivalent on 1976-10-05. Applicant: Storz Instrument Co..

Clearance details

Applicant: Storz Instrument Co.
Product code: Code HNO
Advisory panel: Ophthalmic
Date received: 1976-09-27
Decision date: 1976-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.