VAN DELLEN HEALON CANNULA— 510(k) K873164

Name: FDA 510(k) clearance K873164
Creator: U.S. Food and Drug Administration
Published: 1987-09-04

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.. Device class: 1.

Clearance details

Applicant: Van Dellen, Ltd.
Product code: Code HMX
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1987-08-11
Decision date: 1987-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

Download summary PDF View on FDA.gov ↗

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More clearances from Van Dellen, Ltd.

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K873465 — VAN DELLEN BACTERIA FILTER1988-01-20
K873463 — VAN DELLEN ASPIRATING TUBING1987-11-23
K873464 — VAN DELLEN CANNULA1987-11-23
K873462 — VAN DELLEN ASPIRATOR1987-09-25
K873162 — VAN DELLEN RETROBULBAR NEEDLE1987-09-04

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.