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BELIMED STEAM STERILIZER MST-H

K141879 Class II Abbreviated
Decision Date
2015-06-17
Sponsor / Applicant
Sauter AG

Technical Specification

510(k) Submission ID K141879
Product Code FLE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6880
Decision Date 2015-06-17
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BELIMED STEAM STERILIZER MST-H received FDA 510(k) clearance under submission number K141879, sponsored by Sauter AG. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2015-06-17.

Classification & Regulation

This clearance is catalogued under FDA product code FLE and 21 CFR 880.6880, within the General Hospital review panel as a Class II device.