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FDA 510(k)

V-CATH BREAKAWAY NEEDLE INTRODUCER

K-Number: K945473 · 1995-01-20

ApplicantHdc Corp.
Decision Date1995-01-20
Product CodeKZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

V-CATH BREAKAWAY NEEDLE INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1995-01-20 under 510(k) number K945473. The device is classified under product code KZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-CATH BREAKAWAY NEEDLE INTRODUCER?

V-CATH BREAKAWAY NEEDLE INTRODUCER is a medical device that received FDA 510(k) clearance on 1995-01-20. The listed applicant is Hdc Corp.. The 510(k) number is K945473.

When did V-CATH BREAKAWAY NEEDLE INTRODUCER receive FDA 510(k) clearance?

V-CATH BREAKAWAY NEEDLE INTRODUCER received FDA 510(k) clearance on 1995-01-20, under 510(k) number K945473.

Who is the listed applicant for V-CATH BREAKAWAY NEEDLE INTRODUCER?

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 V-CATH BREAKAWAY NEEDLE INTRODUCER?

The FDA product code for V-CATH BREAKAWAY NEEDLE INTRODUCER is KZH.

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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 BGK033853MODIFICATION TO V-CATH POLY PICCK032404SELDINGER 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'S

View all 30 devices →

Related Devices (Code: KZH)

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.

K243232GripMateSynthon Hispania S.L.K213429AccuSert Needle InserterEmed Technologies CorporationK163400Orbit InserterYpsomed AGK160860MiniMed Quick-serterMedtronic MinimedK124026LOBSTER AUTO-INJECTORScandinavian Health LimitedK122837AUTOJECT 2 FOR GLASSY SYRINGEOwen Mumford, Ltd.

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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