meddevicedb.com FDA Device Reference

Automatic Tissue Processing Unit

K172717 Class II Traditional
Decision Date
2018-05-25
Sponsor / Applicant
Bsl Co.

Technical Specification

510(k) Submission ID K172717
Product Code MUU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5040
Decision Date 2018-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Automatic Tissue Processing Unit received FDA 510(k) clearance under submission number K172717, sponsored by Bsl Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2018-05-25.

Classification & Regulation

This clearance is catalogued under FDA product code MUU and 21 CFR 878.5040, within the General, Plastic Surgery review panel as a Class II device.