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FDA 510(k)

VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT

K-Number: K881504 · 1988-06-22

ApplicantHdc Corp.
Decision Date1988-06-22
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1988-06-22 under 510(k) number K881504. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT?

VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT is a medical device that received FDA 510(k) clearance on 1988-06-22. The listed applicant is Hdc Corp.. The 510(k) number is K881504.

When did VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT receive FDA 510(k) clearance?

VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT received FDA 510(k) clearance on 1988-06-22, under 510(k) number K881504.

Who is the listed applicant for VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT?

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 VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT?

The FDA product code for VEN-A-CATH PERCUTANEOUS VENOUS CATHETER KIT is DQY.

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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

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Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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