meddevicedb.com FDA Device Reference

TISSUE SPECTROSCOPE

K992529 Class II Traditional
Decision Date
2000-11-17
Sponsor / Applicant
Vital Medical , Ltd.

Technical Specification

510(k) Submission ID K992529
Product Code DPW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2100
Decision Date 2000-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TISSUE SPECTROSCOPE received FDA 510(k) clearance under submission number K992529, sponsored by Vital Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code DPW and 21 CFR 870.2100, within the Cardiovascular review panel as a Class II device.