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NOVA SAFE SCALP VEIN BLOOD COLLECTION SET

K090502 Class II Traditional
Decision Date
2009-03-10
Sponsor / Applicant
U.S. Safety Syringes Co., Inc.

Technical Specification

510(k) Submission ID K090502
Product Code FOZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5200
Decision Date 2009-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVA SAFE SCALP VEIN BLOOD COLLECTION SET received FDA 510(k) clearance under submission number K090502, sponsored by U.S. Safety Syringes Co., 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 2009-03-10.

Classification & Regulation

This clearance is catalogued under FDA product code FOZ and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.