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FDA 510(k)

MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT

K-Number: K910022 · 1991-04-02

ApplicantMedical Marketing Group
Decision Date1991-04-02
Product CodeFCM
Advisory CommitteeGU
DecisionUnknown

Device Summary

MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT 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 1991-04-02 under 510(k) number K910022. The device is classified under product code FCM. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT?

MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT is a medical device that received FDA 510(k) clearance on 1991-04-02. The listed applicant is Medical Marketing Group. The 510(k) number is K910022.

When did MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT receive FDA 510(k) clearance?

MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT received FDA 510(k) clearance on 1991-04-02, under 510(k) number K910022.

Who is the listed applicant for MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT?

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 MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT?

The FDA product code for MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT is FCM.

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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.

K884819O'NEIL URINARY CATHETER INTRODUCERK874682MMG CATHETER PLUG W/DRAINAGE TUBE COVERK871999MMG URO-SELF CATHETERK863912THE MMG 5 IN 1 CONNECTORK840838MMG CONNECTIVE TUBINGK821168DISPOSABLE URINARY LEGBAG W/STRAP

View all 11 devices →

Related Devices (Code: FCM)

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.

K254076BD Touchless™ Plus Unisex Pre-Lubricated Urethral Catheter KitC.R. Bard, Inc.K250891Cure Catheter Insertion Kit (K1); Cure Catheter Insertion Kit (K2); Cure Catheter Insertion Kit (K2-90); Cure Catheter Insertion Kit (K3); Cure Hydrophilic Catheter Kit (HM12UK); Cure Hydrophilic Catheter Kit (HM14UK); Cure Hydrophilic Catheter Kit (HM16UK); Cure Pocket Catheter Kit (M14UK); Cure Catheter Closed System Kit (CS8); Cure Catheter Closed System Kit (CS10); Cure Catheter Closed System Kit (CS12); Cure Catheter Closed System Kit (CS14); Cure Catheter Closed System Kit (CS14CConvatec LimitedK223821Self-Cath Closed SystemColoplastK082831AMSELF CLOSED CATHETERIZATION SYSTEMAmsino International, Inc.K070939SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEMColoplast Manufacturing Us, LLCK070048GUARDIAN CATHETER-INFANT URINARY COLLECTION KITMarian Medical, 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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