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SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR

K063240 Class II Special
Decision Date
2006-11-21
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K063240
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2006-11-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR received FDA 510(k) clearance under submission number K063240, sponsored by C.R. Bard, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2006-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.