TK Intravascular Administration Set— 510(k) K191640

Substantially Equivalent

Anhui Tiankang Medical Technology Co., Ltd.

FDA 510(k) clearance K191640 for TK Intravascular Administration Set, Substantially Equivalent on 2020-08-26. Applicant: Anhui Tiankang Medical Technology Co., Ltd..

Clearance details

Applicant: Anhui Tiankang Medical Technology Co., Ltd.
Product code: Code FPA
Advisory panel: General Hospital
Date received: 2019-06-19
Decision date: 2020-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tianchang, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

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.