Baxter Baffled Tee Adapter

FDA 510(k) K895014 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK895014

Submission

Device name
Baxter Baffled Tee Adapter
Applicant
Baxter Healthcare Corp
Valencia, CA, US
Received
August 8, 1989
Decision date
October 30, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BZA – Connector, Airway (Extension)
Device class
Class I (low risk)
Regulation
21 CFR 868.5810
Specialty
Anesthesiology

Other 510(k)s with product code BZA

510(k)DeviceApplicantDecision
K083702Trach-AssistBZA · Traditional Mergenet Medical03/05/2009SE
K954383Sureloc Circuit ConnectorBZA · Traditional Polamedco, Inc.12/22/1995SE
K954197Disposable Flex TubeBZA · Traditional Engstrom Medical10/26/1995SE
K953786Unicor, Inc. Connectors & Airway ExtensionsBZA · Traditional Unicor, Inc.09/19/1995SE
K952824Neo-Link, Disposable Neonatal Air Way ConnectorBZA · Traditional Intertex Medical, Inc.07/20/1995SE
K951345Disposable Airway Connectors for Gas SamplingBZA · Traditional Catheter Research, Inc.04/14/1995SE
K944532Prima, Inc. Ventilator HosesBZA · Traditional Prima, Inc.12/02/1994SE
K944535Prima, Inc. Gas Sampling Lines and ConnectorsBZA · Traditional Prima, Inc.11/29/1994SE
K944534Prima, Inc. Connectors and Airway ExtensionsBZA · Traditional Prima, Inc.11/29/1994SE
K942392Airway Connector with Flex TubeBZA · Traditional Mallinckrodt Medical08/22/1994SE

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Questions and answers

When was Baxter Baffled Tee Adapter cleared by the FDA?

Baxter Baffled Tee Adapter (K895014) received a 510(k) decision of Substantially Equivalent on October 30, 1989, 83 days after the submission was received.

What is the product code of K895014?

The FDA product code is BZA – Connector, Airway (Extension), a Class I (low risk) device regulated under 21 CFR 868.5810.