meddevicedb.com FDA Device Reference

PICC-FIX

K911070 Class I Traditional
Decision Date
1991-07-05
Sponsor / Applicant
Sorex Medical

Technical Specification

510(k) Submission ID K911070
Product Code KMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5210
Decision Date 1991-07-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICC-FIX received FDA 510(k) clearance under submission number K911070, sponsored by Sorex Medical. 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 1991-07-05.

Classification & Regulation

This clearance is catalogued under FDA product code KMK and 21 CFR 880.5210, within the General Hospital review panel as a Class I device.