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EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET

K022406 Class II Traditional
Decision Date
2002-09-30
Sponsor / Applicant
Exelint Intl. Co.

Technical Specification

510(k) Submission ID K022406
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2002-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET received FDA 510(k) clearance under submission number K022406, sponsored by Exelint Intl. Co.. 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 2002-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.