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FDA 510(k)

VANISHPOINT I.V. CATHETER

K-Number: K081420 · 2008-11-07

ApplicantRetractable Technologies, Inc.
Decision Date2008-11-07
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VANISHPOINT I.V. CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Retractable Technologies, Inc.. It received FDA 510(k) clearance on 2008-11-07 under 510(k) number K081420. 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 VANISHPOINT I.V. CATHETER?

VANISHPOINT I.V. CATHETER is a medical device that received FDA 510(k) clearance on 2008-11-07. The listed applicant is Retractable Technologies, Inc.. The 510(k) number is K081420.

When did VANISHPOINT I.V. CATHETER receive FDA 510(k) clearance?

VANISHPOINT I.V. CATHETER received FDA 510(k) clearance on 2008-11-07, under 510(k) number K081420.

Who is the listed applicant for VANISHPOINT I.V. CATHETER?

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

What is the FDA product code for VANISHPOINT I.V. CATHETER?

The FDA product code for VANISHPOINT I.V. CATHETER is FOZ.

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Other records listing Retractable Technologies, 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.

K202325EasyPoint Blood Collection PlusK122355VANISHPOINT BLOOD COLLECTION SETK112512VANISHPOINT BLOOD COLLECTION SETK101708PATIENT SAFE LUER CAPK072654PATIENT SAFE SYRINGEK051355VANISHPOINT I.V. CATHETER

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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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