Flex-Elbow

FDA 510(k) K912652 · Vital Signs, Inc.

Substantially Equivalent

510(k) numberK912652

Submission

Device name
Flex-Elbow
Applicant
Vital Signs, Inc.
Totowa, NJ, US
Received
June 17, 1991
Decision date
October 10, 1991
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

Other 510(k)s with product code BZA

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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 Flex-Elbow cleared by the FDA?

Flex-Elbow (K912652) received a 510(k) decision of Substantially Equivalent on October 10, 1991, 115 days after the submission was received.

What is the product code of K912652?

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