FDA 510(k)

STERILE HICHMAN/BROVIAC INJECTION CAP

K-Number: K840846 · 1984-07-06

Decision Date1984-07-06

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERILE HICHMAN/BROVIAC INJECTION CAP is the device name listed in this FDA 510(k) record. The listed applicant is Evermed, Inc.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K840846. 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 STERILE HICHMAN/BROVIAC INJECTION CAP?

STERILE HICHMAN/BROVIAC INJECTION CAP is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Evermed, Inc.. The 510(k) number is K840846.

When did STERILE HICHMAN/BROVIAC INJECTION CAP receive FDA 510(k) clearance?

STERILE HICHMAN/BROVIAC INJECTION CAP received FDA 510(k) clearance on 1984-07-06, under 510(k) number K840846.

Who is the listed applicant for STERILE HICHMAN/BROVIAC INJECTION CAP?

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 STERILE HICHMAN/BROVIAC INJECTION CAP?

The FDA product code for STERILE HICHMAN/BROVIAC INJECTION CAP is LJS.

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Other records listing Evermed, Inc. as applicant

K840529STEIGER TUNNELING INSTRUMENT 285 K830256NON-STERILE BROVIAC PARENTERAL ALIMI-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.