FDA 510(k)

NON-STERILE BROVIAC PARENTERAL ALIMI-

K-Number: K830256 · 1983-03-01

Decision Date1983-03-01

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NON-STERILE BROVIAC PARENTERAL ALIMI- is the device name listed in this FDA 510(k) record. The listed applicant is Evermed, Inc.. It received FDA 510(k) clearance on 1983-03-01 under 510(k) number K830256. 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 NON-STERILE BROVIAC PARENTERAL ALIMI-?

NON-STERILE BROVIAC PARENTERAL ALIMI- is a medical device that received FDA 510(k) clearance on 1983-03-01. The listed applicant is Evermed, Inc.. The 510(k) number is K830256.

When did NON-STERILE BROVIAC PARENTERAL ALIMI- receive FDA 510(k) clearance?

NON-STERILE BROVIAC PARENTERAL ALIMI- received FDA 510(k) clearance on 1983-03-01, under 510(k) number K830256.

Who is the listed applicant for NON-STERILE BROVIAC PARENTERAL ALIMI-?

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

What is the FDA product code for NON-STERILE BROVIAC PARENTERAL ALIMI-?

The FDA product code for NON-STERILE BROVIAC PARENTERAL ALIMI- is LJS.

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Other records listing Evermed, Inc. as applicant

K840846STERILE HICHMAN/BROVIAC INJECTION CAP K840529STEIGER TUNNELING INSTRUMENT 285 K830406NON-STERILE CATHETER REPAIR KITS K830233NON-STERILE,SINGLE/SOUBLE LUMEN-CATH K830257NON-STERILE PERITONEAL ACCESS CATHET-

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

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