Neo-Link, Disposable Neonatal Air Way Connector

FDA 510(k) K952824 · Intertex Medical, Inc.

Substantially Equivalent

510(k) numberK952824

Submission

Device name
Neo-Link, Disposable Neonatal Air Way Connector
Applicant
Intertex Medical, Inc.
New Canaan, CT, US
Received
June 20, 1995
Decision date
July 20, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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

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K954197Disposable Flex TubeBZA · Traditional Engstrom Medical10/26/1995SE
K953786Unicor, Inc. Connectors & Airway ExtensionsBZA · Traditional Unicor, Inc.09/19/1995SE
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
K941026Thayer Mask to Mouthpiece Adapter/ConnectorBZA · Traditional Thayer Medical Corp.08/18/1994SE

More from Thayer Medical Corp.

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K830711Trachestomy & Nasal Suctioning Kit #-GBZ · Traditional 05/02/1983SE

Questions and answers

When was Neo-Link, Disposable Neonatal Air Way Connector cleared by the FDA?

Neo-Link, Disposable Neonatal Air Way Connector (K952824) received a 510(k) decision of Substantially Equivalent on July 20, 1995, 30 days after the submission was received.

What is the product code of K952824?

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