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FDA 510(k)

3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH

K-Number: K926331 · 1994-03-07

ApplicantBard Access Systems, Inc.
Decision Date1994-03-07
Product CodeLJS
Advisory CommitteeHO
DecisionUnknown

Device Summary

3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH 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 1994-03-07 under 510(k) number K926331. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the 3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH?

3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Bard Access Systems, Inc.. The 510(k) number is K926331.

When did 3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH receive FDA 510(k) clearance?

3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH received FDA 510(k) clearance on 1994-03-07, under 510(k) number K926331.

Who is the listed applicant for 3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH?

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 3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH?

The FDA product code for 3.0 FR GROSHONG PERIPHER INSERT CENT VENOUS CATH is LJS.

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Other records listing Bard Access Systems, Inc. as applicant

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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

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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