meddevicedb.com FDA Device Reference

MEDICAL MAGNETIC TAPE RECORDER

K102111 Class II Traditional
Decision Date
2010-12-07
Sponsor / Applicant
Wpr Medical AS

Technical Specification

510(k) Submission ID K102111
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2010-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICAL MAGNETIC TAPE RECORDER received FDA 510(k) clearance under submission number K102111, sponsored by Wpr Medical AS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.