Double-Swivel Connector

FDA 510(k) K850964 · Sheridan Catheter Corp.

Substantially Equivalent

510(k) numberK850964

Submission

Device name
Double-Swivel Connector
Applicant
Sheridan Catheter Corp.
Argyle, NY, US
Received
March 8, 1985
Decision date
May 14, 1985
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

More from Mallinckrodt Medical

510(k)DeviceDecision
K922894Lazer-Trach Tracheal TubeBTR · Traditional 05/07/1993SE
K897046Laser Resistant Tracheal TubeCBI · Traditional 03/23/1990SE
K890823Accessory to Clinical Electronic ThermometerFLL · Traditional 05/05/1989SE
K884765Clinical Electronic ThermometersFLL · Traditional 02/16/1989SE
K882918Kim Naso-Intestinal TubeKNT · Traditional 12/05/1988SE
K882127Clinical Electronic ThermometersFLL · Traditional 08/04/1988SE
K881368Clinical Electonic ThermometersFLL · Traditional 07/13/1988SE
K881293Sheridan Electrosurgery Protection FilterBZT · Traditional 06/16/1988SE
K881873Introduction/Drainage Catheter & AccessGBS · Traditional 05/18/1988SE
K880960Ndyag Laser Tracheal TubeBTR · Traditional 04/29/1988SE

Questions and answers

When was Double-Swivel Connector cleared by the FDA?

Double-Swivel Connector (K850964) received a 510(k) decision of Substantially Equivalent on May 14, 1985, 67 days after the submission was received.

What is the product code of K850964?

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