meddevicedb.com FDA Device Reference

HRV ACQUIRE

K092809 Class II Abbreviated
Decision Date
2010-10-19
Sponsor / Applicant
Wr Medical Electronics Co.

Technical Specification

510(k) Submission ID K092809
Product Code DRT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2010-10-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HRV ACQUIRE received FDA 510(k) clearance under submission number K092809, sponsored by Wr Medical Electronics Co.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.