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FDA 510(k)

INTRAVENOUS CATHETER PLACEMENT UNIT &

K-Number: K823017 · 1982-11-01

ApplicantAccess Devices, Inc.
Decision Date1982-11-01
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS CATHETER PLACEMENT UNIT & is the device name listed in this FDA 510(k) record. The listed applicant is Access Devices, Inc.. It received FDA 510(k) clearance on 1982-11-01 under 510(k) number K823017. 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 INTRAVENOUS CATHETER PLACEMENT UNIT &?

INTRAVENOUS CATHETER PLACEMENT UNIT & is a medical device that received FDA 510(k) clearance on 1982-11-01. The listed applicant is Access Devices, Inc.. The 510(k) number is K823017.

When did INTRAVENOUS CATHETER PLACEMENT UNIT & receive FDA 510(k) clearance?

INTRAVENOUS CATHETER PLACEMENT UNIT & received FDA 510(k) clearance on 1982-11-01, under 510(k) number K823017.

Who is the listed applicant for INTRAVENOUS CATHETER PLACEMENT UNIT &?

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

What is the FDA product code for INTRAVENOUS CATHETER PLACEMENT UNIT &?

The FDA product code for INTRAVENOUS CATHETER PLACEMENT UNIT & is FOZ.

Related Clinical Trials

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.

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Other records listing Access Devices, Inc. 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.

K823758CENTRAL VEIN CATHERIZATION KITK822834ACCESS PERCUTANEOUS INTRODUCER SET

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

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

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