MODEL C2100-SERIES OPHTHALMIC CRYOPROBE— 510(k) K810409

Substantially Equivalent

Valleylab, Inc.

FDA 510(k) clearance K810409 for MODEL C2100-SERIES OPHTHALMIC CRYOPROBE, Substantially Equivalent on 1981-03-20. Applicant: Valleylab, Inc..

Clearance details

Applicant: Valleylab, Inc.
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 1981-02-18
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code GEH

product code GEH

Death: 25
Injury: 351
Malfunction: 901
Total: 1,277

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.