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FDA 510(k)

SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES

K-Number: K061240 · 2006-06-02

ApplicantLucent Medical Systems
Decision Date2006-06-02
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Lucent Medical Systems. It received FDA 510(k) clearance on 2006-06-02 under 510(k) number K061240. 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 TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES?

SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2006-06-02. The listed applicant is Lucent Medical Systems. The 510(k) number is K061240.

When did SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES receive FDA 510(k) clearance?

SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES received FDA 510(k) clearance on 2006-06-02, under 510(k) number K061240.

Who is the listed applicant for SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES?

The FDA 510(k) record lists Lucent Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES?

The FDA product code for SHERLOCK TIP LOCATION SYSTEM (TLS) DETECTOR AND ACCESSORIES is LJS.

Related Clinical Trials

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Other records listing Lucent Medical Systems 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.

K000997ZORTRAN DETECTOR

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.

K260929Neonav ECG Tip Location SystemNavi Medical TechnologiesK252373BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve TechnologySpectrum VascularK252792PM2™ System with ECGuide™ ConnectorPiccolo Medical, Inc.K243458HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (70002302); HydroPICC 5Fr Dual Lumen Marked catheter - Maximal Barrier kit (70002304); HydrAccess Vascular, Inc.K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)Access Vascular, Inc.K243484PM2+ System and SmartPICC StyletPiccolo Medical, Inc.

Official Source

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

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