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FDA 510(k)

MMG URO-SELF CATHETER

K-Number: K871999 · 1987-08-25

ApplicantMedical Marketing Group
Decision Date1987-08-25
Product CodeGBM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MMG URO-SELF CATHETER 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 1987-08-25 under 510(k) number K871999. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMG URO-SELF CATHETER?

MMG URO-SELF CATHETER is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Medical Marketing Group. The 510(k) number is K871999.

When did MMG URO-SELF CATHETER receive FDA 510(k) clearance?

MMG URO-SELF CATHETER received FDA 510(k) clearance on 1987-08-25, under 510(k) number K871999.

Who is the listed applicant for MMG URO-SELF CATHETER?

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 URO-SELF CATHETER?

The FDA product code for MMG URO-SELF CATHETER is GBM.

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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.

K910022MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KITK884819O'NEIL URINARY CATHETER INTRODUCERK874682MMG CATHETER PLUG W/DRAINAGE TUBE COVERK863912THE MMG 5 IN 1 CONNECTORK840838MMG CONNECTIVE TUBINGK821168DISPOSABLE URINARY LEGBAG W/STRAP

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Related Devices (Code: GBM)

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.

K241734Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter CompactWell Lead Medical Co., Ltd.K213283GentleCath Air for Men Hydrophilic Intermittent Urinary CatheterConvatec LimitedK211436Intermittent Catheter (Not Finalized)Hollister IncorporatedK200820SpeediCath Compact SetColoplastK192904SpeediCath Compact SetColoplastK200142SpeediCath SoftColoplast

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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