KERAVISION VACUUM RING SYSTEM— 510(k) K984540

Substantially Equivalent

Keravision, Inc.

FDA 510(k) clearance K984540 for KERAVISION VACUUM RING SYSTEM, Substantially Equivalent on 1999-04-28. Applicant: Keravision, Inc..

Clearance details

Applicant: Keravision, Inc.
Product code: Code HNO
Advisory panel: Ophthalmic
Date received: 1998-12-21
Decision date: 1999-04-28
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Washington, DC, 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.