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MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER

K953335 Class II Traditional
Decision Date
1996-01-23
Sponsor / Applicant
Micro Therapeutics, Inc.

Technical Specification

510(k) Submission ID K953335
Product Code FOZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5200
Decision Date 1996-01-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER received FDA 510(k) clearance under submission number K953335, sponsored by Micro Therapeutics, 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 1996-01-23.

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.