meddevicedb.com FDA Device Reference

BP LIMBO XL, BPTANGO XL, BP SALSA XL

K072752 Class II Traditional
Decision Date
2008-10-31
Sponsor / Applicant
Datadancer Medical Systems

Technical Specification

510(k) Submission ID K072752
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2008-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BP LIMBO XL, BPTANGO XL, BP SALSA XL received FDA 510(k) clearance under submission number K072752, sponsored by Datadancer Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.