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LIFE SOUND SENSOR

K952651 Class I Traditional
Decision Date
1995-09-19
Sponsor / Applicant
Flowscan, Inc.

Technical Specification

510(k) Submission ID K952651
Product Code DQC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2390
Decision Date 1995-09-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFE SOUND SENSOR received FDA 510(k) clearance under submission number K952651, sponsored by Flowscan, 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 1995-09-19.

Classification & Regulation

This clearance is catalogued under FDA product code DQC and 21 CFR 870.2390, within the Cardiovascular review panel as a Class I device.