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FDA 510(k)

IV CATHETER AND OBTURATOR

K-Number: K941429 · 1995-01-04

ApplicantBecton Dickinson Vascular Access, Inc.
Decision Date1995-01-04
Product CodeFOS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV CATHETER AND OBTURATOR 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 1995-01-04 under 510(k) number K941429. The device is classified under product code FOS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV CATHETER AND OBTURATOR?

IV CATHETER AND OBTURATOR is a medical device that received FDA 510(k) clearance on 1995-01-04. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K941429.

When did IV CATHETER AND OBTURATOR receive FDA 510(k) clearance?

IV CATHETER AND OBTURATOR received FDA 510(k) clearance on 1995-01-04, under 510(k) number K941429.

Who is the listed applicant for IV CATHETER AND OBTURATOR?

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 IV CATHETER AND OBTURATOR?

The FDA product code for IV CATHETER AND OBTURATOR is FOS.

Related Clinical Trials

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Other records listing Becton Dickinson Vascular Access, 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.

K971339INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERSK970259E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SETK964049FIRST MIDCATH CATHETER WITH DUAL LUMENSK964050FIRST MIDCATH CATHETERK964048FIRST MIDCATH CATHETER KITK954906FIRST PICC INTRODUCER CATHETER

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Related Devices (Code: FOS)

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.

K201697Umbilical Vessels CatheterHaolang Medical USA CorporationK130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Covidien Lp, Formerly Registered AS KendallK120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETERFootprint Medical, Inc.K091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENFootprint MedicalK091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERFootprint MedicalK081515NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0Neomed, 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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