TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML)— 510(k) K023458

Substantially Equivalent

Taiject Medical Device Co., Ltd.

FDA 510(k) clearance K023458 for TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML), Substantially Equivalent on 2002-11-07. Applicant: Taiject Medical Device Co., Ltd.. Device class: 2.

Clearance details

Applicant
Taiject Medical Device Co., Ltd.
Product code
Code MEG
Device class
Class 2
Regulation
21 CFR 880.5860
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Irvine, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code MEG

product code MEG
Malfunction
1,373
Other
1
Total
1,374

Source: openFDA MAUDE database, through . 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.