meddevicedb.com FDA Device Reference

ROTATING ADAPTERS

K140475 Class II Traditional
Decision Date
2014-04-16
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K140475
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 2014-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROTATING ADAPTERS received FDA 510(k) clearance under submission number K140475, sponsored by Merit Medical Systems, 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 2014-04-16.

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.