Shinva Ande Healthcare Apparatus Co., Ltd.

FDA Regulatory Profile

Shinva Ande Healthcare Apparatus Co., Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 23, 2022.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K201460Closed System Transfer DeviceNovember 23, 2022
K220057Disposable Sterile Syringe with permanently attached needle; Auto-disable Syringe for Fixed-dose ImmOctober 7, 2022
K211484Disposable Sterile Syringe with Safety Needle; Disposable Sterile Syringe with Needle; Disposable StMarch 1, 2022
K202060Disposable IV catheterJuly 23, 2021
K193657Disposable Enteral Feeding Syringe with Enfit ConnectorSeptember 12, 2020
K162601Infusion Set for Single UseMay 31, 2017