VAN DELLEN HEALON CANNULA— 510(k) K873164

Substantially Equivalent

Van Dellen, Ltd.

FDA 510(k) clearance K873164 for VAN DELLEN HEALON CANNULA, Substantially Equivalent on 1987-09-04. Applicant: Van Dellen, Ltd..

Clearance details

Applicant: Van Dellen, Ltd.
Product code: Code HMX
Advisory panel: Ophthalmic
Date received: 1987-08-11
Decision date: 1987-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

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Adverse events under product code HMX

product code HMX

Other: 1
Total: 1

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.