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FDA 510(k)

UNIVERSAL OXYGEN TUBING CONNECTOR

K-Number: K840790 · 1984-03-30

ApplicantCherry Plastics, Inc.
Decision Date1984-03-30
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL OXYGEN TUBING CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Cherry Plastics, Inc.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K840790. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL OXYGEN TUBING CONNECTOR?

UNIVERSAL OXYGEN TUBING CONNECTOR is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Cherry Plastics, Inc.. The 510(k) number is K840790.

When did UNIVERSAL OXYGEN TUBING CONNECTOR receive FDA 510(k) clearance?

UNIVERSAL OXYGEN TUBING CONNECTOR received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840790.

Who is the listed applicant for UNIVERSAL OXYGEN TUBING CONNECTOR?

The FDA 510(k) record lists Cherry Plastics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL OXYGEN TUBING CONNECTOR?

The FDA product code for UNIVERSAL OXYGEN TUBING CONNECTOR is BYX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cherry Plastics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K840789BITESTICK BLOCK

Related Devices (Code: BYX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K011134OXYGEN SUPPLY TUBING, MODEL 1115Hudson Respiratory Care, Inc.K955656NORTH STATE PLASTICS AEROSOL TEENorth State Plastics, Inc.K943110GAS SAMPLING INTERFACESCoast Medical, Inc.K935835BUSSE PLASTIC TUBING CONNECTORS AND ACCESSORIESBusse Hospital Disposables, Inc.K931033MF CHEMETRON STYLE MEDICAL GAS WALL OUTLETSMedical Fittings, Inc.K931043MF OHMEDA STYLE MEDICAL GAS WALL OUTLETSMedical Fittings, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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