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FDA 510(k)

SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR

K-Number: K063240 · 2006-11-21

ApplicantC.R. Bard, Inc.
Decision Date2006-11-21
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2006-11-21 under 510(k) number K063240. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR?

SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR is a medical device that received FDA 510(k) clearance on 2006-11-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K063240.

When did SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR receive FDA 510(k) clearance?

SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR received FDA 510(k) clearance on 2006-11-21, under 510(k) number K063240.

Who is the listed applicant for SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR?

The FDA product code for SHERLOCK TLS STYLET, SHERLOCK TLS DETECTOR is LJS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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