meddevicedb.com FDA Device Reference

REPROCESSED TROCARS

K062497 Class II Traditional
Decision Date
2007-01-31
Sponsor / Applicant
Ascent Healthcare Solutions

Technical Specification

510(k) Submission ID K062497
Product Code NLM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2007-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REPROCESSED TROCARS received FDA 510(k) clearance under submission number K062497, sponsored by Ascent Healthcare Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2007-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code NLM and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.