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ROBINSON MEDSURG QUICKSCREW RACK

K093800 Class II Traditional
Decision Date
2010-06-16
Sponsor / Applicant
Robinson Medsurg, LLC

Technical Specification

510(k) Submission ID K093800
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2010-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROBINSON MEDSURG QUICKSCREW RACK received FDA 510(k) clearance under submission number K093800, sponsored by Robinson Medsurg, LLC. 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 2010-06-16.

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.