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FDA 510(k)

Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly

K-Number: K222232 · 2022-08-24

Decision Date2022-08-24
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly is the device name listed in this FDA 510(k) record. The listed applicant is Bard Access Systems, Inc.. It received FDA 510(k) clearance on 2022-08-24 under 510(k) number K222232. 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 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly?

Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly is a medical device that received FDA 510(k) clearance on 2022-08-24. The listed applicant is Bard Access Systems, Inc.. The 510(k) number is K222232.

When did Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly receive FDA 510(k) clearance?

Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly received FDA 510(k) clearance on 2022-08-24, under 510(k) number K222232.

Who is the listed applicant for Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly?

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

What is the FDA product code for Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly?

The FDA product code for Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly is LJS.

Other records listing Bard Access Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: LJS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.