meddevicedb.com FDA Device Reference

CELL-TISSUE CONVERTER (CTC) SYRINGE WITH NEEDLE

K110112 Class II Traditional
Decision Date
2011-04-20
Sponsor / Applicant
Rongshan LI

Technical Specification

510(k) Submission ID K110112
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2011-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CELL-TISSUE CONVERTER (CTC) SYRINGE WITH NEEDLE received FDA 510(k) clearance under submission number K110112, sponsored by Rongshan LI. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.