VIADERM— 510(k) K914024

Substantially Equivalent

Abs Life Sciences

FDA 510(k) clearance K914024 for VIADERM, Substantially Equivalent on 1991-12-04. Applicant: Abs Life Sciences.

Clearance details

Applicant: Abs Life Sciences
Product code: Code KGN
Advisory panel: Unknown
Date received: 1991-09-10
Decision date: 1991-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

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Adverse events under product code KGN

product code KGN

Other: 2
Total: 2

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.