meddevicedb.com FDA Device Reference

SUSTAIN

K131866 Class II Abbreviated
Decision Date
2014-05-01
Sponsor / Applicant
Hollender Sustainable Brands, LLC

Technical Specification

510(k) Submission ID K131866
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2014-05-01
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUSTAIN received FDA 510(k) clearance under submission number K131866, sponsored by Hollender Sustainable Brands, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2014-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code HIS and 21 CFR 884.5300, within the Obstetrics/Gynecology review panel as a Class II device.