Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

THE MMG 5 IN 1 CONNECTOR

K-Number: K863912 · 1986-10-27

ApplicantMedical Marketing Group
Decision Date1986-10-27
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE MMG 5 IN 1 CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing Group. It received FDA 510(k) clearance on 1986-10-27 under 510(k) number K863912. 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 THE MMG 5 IN 1 CONNECTOR?

THE MMG 5 IN 1 CONNECTOR is a medical device that received FDA 510(k) clearance on 1986-10-27. The listed applicant is Medical Marketing Group. The 510(k) number is K863912.

When did THE MMG 5 IN 1 CONNECTOR receive FDA 510(k) clearance?

THE MMG 5 IN 1 CONNECTOR received FDA 510(k) clearance on 1986-10-27, under 510(k) number K863912.

Who is the listed applicant for THE MMG 5 IN 1 CONNECTOR?

The FDA 510(k) record lists Medical Marketing Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE MMG 5 IN 1 CONNECTOR?

The FDA product code for THE MMG 5 IN 1 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 Medical Marketing Group 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.

K910022MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KITK884819O'NEIL URINARY CATHETER INTRODUCERK874682MMG CATHETER PLUG W/DRAINAGE TUBE COVERK871999MMG URO-SELF CATHETERK840838MMG CONNECTIVE TUBINGK821168DISPOSABLE URINARY LEGBAG W/STRAP

View all 11 devices →

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.

↑