VENTRE/SEP T3 TEST SET— 510(k) K791588

Substantially Equivalent

Ventrex Laboratories, Inc.

FDA 510(k) clearance K791588 for VENTRE/SEP T3 TEST SET, Substantially Equivalent on 1979-09-27. Applicant: Ventrex Laboratories, Inc..

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code CDP
Advisory panel: Clinical Chemistry
Date received: 1979-08-17
Decision date: 1979-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code CDP

product code CDP

Malfunction: 647
Total: 647

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.