RITRACT SAFETY SYRINGE— 510(k) K060002

Substantially Equivalent

Ritract , Ltd.

FDA 510(k) clearance K060002 for RITRACT SAFETY SYRINGE, Substantially Equivalent on 2006-06-02. Applicant: Ritract , Ltd..

Clearance details

Applicant: Ritract , Ltd.
Product code: Code MEG
Advisory panel: General Hospital
Date received: 2006-01-03
Decision date: 2006-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Sydney, New South Wales, AU

Download summary PDF View on FDA.gov ↗

Adverse events under product code MEG

product code MEG

Malfunction: 1,373
Other: 1
Total: 1,374

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.