Tubing, Single Use Oxygen Supply

FDA 510(k) K760220 · Manner Medical Products

Substantially Equivalent

510(k) numberK760220

Submission

Device name
Tubing, Single Use Oxygen Supply
Applicant
Manner Medical Products
Mchenry, IL, US
Received
July 12, 1976
Decision date
August 3, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BYX – Tubing, Pressure And Accessories
Device class
Class I (low risk)
Regulation
21 CFR 868.5860
Specialty
Anesthesiology

Other 510(k)s with product code BYX

510(k)DeviceApplicantDecision
K011134Oxygen Supply Tubing, Model 1115BYX · Traditional Hudson Respiratory Care, Inc.06/13/2001SE
K955656North State Plastics Aerosol TeeBYX · Traditional North State Plastics, Inc.03/06/1996SE
K943110Gas Sampling InterfacesBYX · Traditional Coast Medical, Inc.08/19/1994SE
K935835Busse Plastic Tubing Connectors and AccessoriesBYX · Traditional Busse Hospital Disposables, Inc.01/12/1994SE
K931043MF Ohmeda Style Medical Gas Wall OutletsBYX · Traditional Medical Fittings, Inc.06/01/1993SE
K931033MF Chemetron Style Medical Gas Wall OutletsBYX · Traditional Medical Fittings, Inc.06/01/1993SE
K913422Oxygen Tubing, 81503BYX · Traditional Specialty Packaging Producs, Inc.01/30/1992SE
K914980Hex, Quad, or Rail Block Manifold AccessoriesBYX · Traditional Medical Fittings, Inc.01/21/1992SE
K912763Ohmeda Style Check Units (Female Couplers)BYX · Traditional Medical Fittings, Inc.10/15/1991SE
K905091Various Male Quick Connects.BYX · Traditional Medical Fittings, Inc.03/04/1991SE

More from Medical Fittings, Inc.

510(k)DeviceDecision
K760221I.P.P.B., Dis. W/Manifold/NebulizerCBO · Traditional 08/03/1976SE
K760219Maska, Oxygen Vinyl D-Sp. Single UseBYG · Traditional 08/03/1976SE
K760218Cannulae, Plastic Disposable NasalCAT · Traditional 08/03/1976SE

Questions and answers

When was Tubing, Single Use Oxygen Supply cleared by the FDA?

Tubing, Single Use Oxygen Supply (K760220) received a 510(k) decision of Substantially Equivalent on August 3, 1976, 22 days after the submission was received.

What is the product code of K760220?

The FDA product code is BYX – Tubing, Pressure And Accessories, a Class I (low risk) device regulated under 21 CFR 868.5860.