meddevicedb.com FDA Device Reference

ADAPTER CABLE

K050884 Class II Traditional
Decision Date
2005-05-19
Sponsor / Applicant
Remington Medical, Inc.

Technical Specification

510(k) Submission ID K050884
Product Code DTA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3720
Decision Date 2005-05-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADAPTER CABLE received FDA 510(k) clearance under submission number K050884, sponsored by Remington Medical, 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 2005-05-19.

Classification & Regulation

This clearance is catalogued under FDA product code DTA and 21 CFR 870.3720, within the Cardiovascular review panel as a Class II device.