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FDA 510(k)

NEOSCI MEDICAL ENDOLUMINAL BRUSH

K-Number: K030400 · 2004-12-22

ApplicantNeosci Medical, Inc.
Decision Date2004-12-22
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEOSCI MEDICAL ENDOLUMINAL BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Neosci Medical, Inc.. It received FDA 510(k) clearance on 2004-12-22 under 510(k) number K030400. 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 NEOSCI MEDICAL ENDOLUMINAL BRUSH?

NEOSCI MEDICAL ENDOLUMINAL BRUSH is a medical device that received FDA 510(k) clearance on 2004-12-22. The listed applicant is Neosci Medical, Inc.. The 510(k) number is K030400.

When did NEOSCI MEDICAL ENDOLUMINAL BRUSH receive FDA 510(k) clearance?

NEOSCI MEDICAL ENDOLUMINAL BRUSH received FDA 510(k) clearance on 2004-12-22, under 510(k) number K030400.

Who is the listed applicant for NEOSCI MEDICAL ENDOLUMINAL BRUSH?

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

What is the FDA product code for NEOSCI MEDICAL ENDOLUMINAL BRUSH?

The FDA product code for NEOSCI MEDICAL ENDOLUMINAL BRUSH is LJS.

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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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