meddevicedb.com FDA Device Reference

TORQUE FITTING

K912969 Class II Traditional
Decision Date
1991-11-05
Sponsor / Applicant
Freedom Machine, Inc.

Technical Specification

510(k) Submission ID K912969
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 1991-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TORQUE FITTING received FDA 510(k) clearance under submission number K912969, sponsored by Freedom Machine, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-11-05.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.