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FDA 510(k)

MMG FOLEY CATHETER

K-Number: K840839 · 1984-04-17

ApplicantMedical Technologies of Georgia
Decision Date1984-04-17
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MMG FOLEY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technologies of Georgia. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K840839. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMG FOLEY CATHETER?

MMG FOLEY CATHETER is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Medical Technologies of Georgia. The 510(k) number is K840839.

When did MMG FOLEY CATHETER receive FDA 510(k) clearance?

MMG FOLEY CATHETER received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840839.

Who is the listed applicant for MMG FOLEY CATHETER?

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

What is the FDA product code for MMG FOLEY CATHETER?

The FDA product code for MMG FOLEY CATHETER is KOD.

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Other records listing Medical Technologies of Georgia 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.

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Related Devices (Code: KOD)

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.

K251864Rubber Utility CatheterC.R. Bard, Inc.K220036Wellead Ureteral CatheterWell Lead Medical Co., Ltd.K220730allFlex Ureteral Catheters, Krait Ureteral CathetersAllwin Medical Devices, Inc.K211032Urinary Catheter 12 Fr, Urinary Catheter 16 FrUrogen Pharma, Ltd.K181979Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent CatheterTeleflexmedical, Inc.K180354UroGen Ureteral CatheterUrogen Pharma, Ltd.

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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