meddevicedb.com FDA Device Reference

SYVEKEXCEL

K053300 Class II Traditional
Decision Date
2006-03-28
Sponsor / Applicant
Marine Polymer Technologies, Inc.

Technical Specification

510(k) Submission ID K053300
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2006-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYVEKEXCEL received FDA 510(k) clearance under submission number K053300, sponsored by Marine Polymer Technologies, 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 2006-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.