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Instru-Safe Instrument Protection System

K150540 Class II Traditional
Decision Date
2015-06-22
Sponsor / Applicant
Summit Medical, Inc.

Technical Specification

510(k) Submission ID K150540
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2015-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Instru-Safe Instrument Protection System received FDA 510(k) clearance under submission number K150540, sponsored by Summit Medical, Inc.. 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 2015-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.