VENES CUSTON RX— 510(k) K820484

Substantially Equivalent

Jung Products, Inc.

FDA 510(k) clearance K820484 for VENES CUSTON RX, Substantially Equivalent on 1982-03-18. Applicant: Jung Products, Inc..

Clearance details

Applicant: Jung Products, Inc.
Product code: Code FQL
Advisory panel: General Hospital
Date received: 1982-02-22
Decision date: 1982-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FQL

product code FQL

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.