meddevicedb.com FDA Device Reference

TATCH-IT

K870356 Class II Traditional
Decision Date
1987-06-12
Sponsor / Applicant
Reunion Medical Co.

Technical Specification

510(k) Submission ID K870356
Product Code DRS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2850
Decision Date 1987-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TATCH-IT received FDA 510(k) clearance under submission number K870356, sponsored by Reunion Medical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1987-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code DRS and 21 CFR 870.2850, within the Cardiovascular review panel as a Class II device.