FDA 510(k)

INTIMA POINT GUARD INTRAVASCULAR CATHETER

K-Number: K923702 · 1993-09-22

ApplicantBecton Dickinson Vascular Access, Inc.

Decision Date1993-09-22

Product CodeFOZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

INTIMA POINT GUARD INTRAVASCULAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vascular Access, Inc.. It received FDA 510(k) clearance on 1993-09-22 under 510(k) number K923702. 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 INTIMA POINT GUARD INTRAVASCULAR CATHETER?

INTIMA POINT GUARD INTRAVASCULAR CATHETER is a medical device that received FDA 510(k) clearance on 1993-09-22. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K923702.

When did INTIMA POINT GUARD INTRAVASCULAR CATHETER receive FDA 510(k) clearance?

INTIMA POINT GUARD INTRAVASCULAR CATHETER received FDA 510(k) clearance on 1993-09-22, under 510(k) number K923702.

Who is the listed applicant for INTIMA POINT GUARD INTRAVASCULAR CATHETER?

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

What is the FDA product code for INTIMA POINT GUARD INTRAVASCULAR CATHETER?

The FDA product code for INTIMA POINT GUARD INTRAVASCULAR CATHETER is FOZ.

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Other records listing Becton Dickinson Vascular Access, Inc. as applicant

K971339INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERS K970259E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET K964048FIRST MIDCATH CATHETER KIT K964050FIRST MIDCATH CATHETER K964049FIRST MIDCATH CATHETER WITH DUAL LUMENS K954906FIRST PICC INTRODUCER CATHETER

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Related Devices (Code: FOZ)

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum Vascular K261041ClearSafe Closed SystemMedSource Labs, LLC K260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLC K253235Introcan 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.