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FDA 510(k)

MODIFICATION TO V-CATH POLY PICC

K-Number: K033853 · 2004-01-14

ApplicantHdc Corp.
Decision Date2004-01-14
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO V-CATH POLY PICC is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 2004-01-14 under 510(k) number K033853. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO V-CATH POLY PICC?

MODIFICATION TO V-CATH POLY PICC is a medical device that received FDA 510(k) clearance on 2004-01-14. The listed applicant is Hdc Corp.. The 510(k) number is K033853.

When did MODIFICATION TO V-CATH POLY PICC receive FDA 510(k) clearance?

MODIFICATION TO V-CATH POLY PICC received FDA 510(k) clearance on 2004-01-14, under 510(k) number K033853.

Who is the listed applicant for MODIFICATION TO V-CATH POLY PICC?

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

What is the FDA product code for MODIFICATION TO V-CATH POLY PICC?

The FDA product code for MODIFICATION TO V-CATH POLY PICC is FOZ.

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Other records listing Hdc Corp. as applicant

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.

K071875V-CATH POLY PICCK023342NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BGK032404SELDINGER SAFETY NEEDLE INTRODUCERK022752PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15K022099SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'SK010425EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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