WEISS RETINAL CANNULA— 510(k) K010305

Substantially Equivalent

Micron Surgical, Inc.

FDA 510(k) clearance K010305 for WEISS RETINAL CANNULA, Substantially Equivalent on 2001-05-02. Applicant: Micron Surgical, Inc..

Clearance details

Applicant: Micron Surgical, Inc.
Product code: Code HMX
Advisory panel: Ophthalmic
Date received: 2001-02-01
Decision date: 2001-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Margate, FL, 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.