NEEDLES, CANNULAS, CYSTOTOMES— 510(k) K782169

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K782169 for NEEDLES, CANNULAS, CYSTOTOMES, Substantially Equivalent on 1979-02-13. Applicant: Visitec Co..

Clearance details

Applicant: Visitec Co.
Product code: Code HMX
Advisory panel: Ophthalmic
Date received: 1978-12-29
Decision date: 1979-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.