meddevicedb.com FDA Device Reference

STOP U (Packed Black USA), STOP U (Packed White USA)

K182774 Class II Traditional
Decision Date
2019-06-19
Sponsor / Applicant
Pollogen, Ltd.

Technical Specification

510(k) Submission ID K182774
Product Code PAY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4420
Decision Date 2019-06-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STOP U (Packed Black USA), STOP U (Packed White USA) received FDA 510(k) clearance under submission number K182774, sponsored by Pollogen, Ltd.. 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 2019-06-19.

Classification & Regulation

This clearance is catalogued under FDA product code PAY and 21 CFR 878.4420, within the General, Plastic Surgery review panel as a Class II device.