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Baxter Accuport Central Venous Catheter

by Bentley Laboratories, Inc.

510(k) K874618

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK874618 Date19 Jan 1988ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

Full name
Baxter Accuport(Tm) Central Venous Catheter
510(k) Number
FDA Product Code
DQR
Device Class
Class II
Regulation
21 CFR Part 870.1300
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Baxter Accuport Central Venous Catheter is a cannula and catheter device classified under cardiovascular medical specialties. It is designed to facilitate access to the central venous system for clinical applications.

This device is authorized under FDA 510(k) clearance K874618. It is manufactured by Bentley Laboratories, Inc. and is categorized under regulation number 870.1300.

Other devices from Bentley Laboratories, Inc.

See all devices from Bentley Laboratories, Inc. →

Questions

AI-generated answers, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the primary clinical application of the Baxter Accuport Central Venous Catheter?

    This device is designed to facilitate access to the central venous system, allowing clinicians to perform necessary cardiovascular procedures that require central venous entry.

  • Is the Baxter Accuport Central Venous Catheter authorized for use?

    Yes, this device is authorized under FDA 510(k) clearance K874618, which indicates that it has been found substantially equivalent to other legally marketed devices.

  • Who is the manufacturer of the Accuport Central Venous Catheter?

    The device is manufactured by Bentley Laboratories, Inc., located in Irvine, California.