I.V. START KIT— 510(k) K924811

Unknown

Transidyne General Corp.

FDA 510(k) clearance K924811 for I.V. START KIT, Unknown on 1993-06-17. Applicant: Transidyne General Corp..

Clearance details

Applicant: Transidyne General Corp.
Product code: Code LRS
Advisory panel: General Hospital
Date received: 1992-09-25
Decision date: 1993-06-17
Decision: Unknown
Clearance type: Traditional
Location: Spartanburg, SC, US

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Adverse events under product code LRS

product code LRS

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.