VANISHPOINT BLOOD COLLECTION SET— 510(k) K122355

Substantially Equivalent

Retractable Technologies, Inc.

FDA 510(k) clearance K122355 for VANISHPOINT BLOOD COLLECTION SET, Substantially Equivalent on 2013-08-23. Applicant: Retractable Technologies, Inc..

Clearance details

Applicant: Retractable Technologies, Inc.
Product code: Code JKA
Advisory panel: Clinical Chemistry
Date received: 2012-08-03
Decision date: 2013-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Little Elm, TX, US

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Adverse events under product code JKA

product code JKA

Injury: 455
Malfunction: 26,686
Other: 4
Total: 27,145

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.