K022278

Substantially Equivalent

TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)

Applicant: Taiject Medical Device Co., Ltd.
Product code: MEG
Advisory panel: General Hospital
Date received: 2002-07-15
Decision date: 2002-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

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.