FDA 510(k)

GROSHONG CATHETER, LONG TERM TYPE

K-Number: K831386 · 1983-10-14

Decision Date1983-10-14

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

GROSHONG CATHETER, LONG TERM TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Catheter Technology Corp.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K831386. 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 GROSHONG CATHETER, LONG TERM TYPE?

GROSHONG CATHETER, LONG TERM TYPE is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Catheter Technology Corp.. The 510(k) number is K831386.

When did GROSHONG CATHETER, LONG TERM TYPE receive FDA 510(k) clearance?

GROSHONG CATHETER, LONG TERM TYPE received FDA 510(k) clearance on 1983-10-14, under 510(k) number K831386.

Who is the listed applicant for GROSHONG CATHETER, LONG TERM TYPE?

The FDA 510(k) record lists Catheter Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GROSHONG CATHETER, LONG TERM TYPE?

The FDA product code for GROSHONG CATHETER, LONG TERM TYPE is LJS.

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Other records listing Catheter Technology Corp. as applicant

K880571CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM K871080PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER K871998GROSHONG CV CATHETER REPAIR KIT K860256BRAWN AND GROSHONG CATHETERS K842577CATH-TECH POLYURETHANE UMBILICAL VESS K842147CATH-TECH CHOLANGIOGRAPHY CATHETER

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Related Devices (Code: LJS)

K260929Neonav ECG Tip Location SystemNavi Medical Technologies K252373BioFlo 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 Vascular K252792PM2™ 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.