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TERUMO MICRO TAPERED PEN NEEDLE

K052561 Class II Traditional
Decision Date
2005-11-23
Sponsor / Applicant
Kofu Factory of Terumo Corp.

Technical Specification

510(k) Submission ID K052561
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2005-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TERUMO MICRO TAPERED PEN NEEDLE received FDA 510(k) clearance under submission number K052561, sponsored by Kofu Factory of Terumo Corp.. 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 2005-11-23.

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.