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FDA 510(k)

MMG DISPOSABLE URINARY LEG BAG

K-Number: K800694 · 1980-05-30

Decision Date1980-05-30
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MMG DISPOSABLE URINARY LEG BAG 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 1980-05-30 under 510(k) number K800694. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMG DISPOSABLE URINARY LEG BAG?

MMG DISPOSABLE URINARY LEG BAG is a medical device that received FDA 510(k) clearance on 1980-05-30. The listed applicant is Medical Marketing Group. The 510(k) number is K800694.

When did MMG DISPOSABLE URINARY LEG BAG receive FDA 510(k) clearance?

MMG DISPOSABLE URINARY LEG BAG received FDA 510(k) clearance on 1980-05-30, under 510(k) number K800694.

Who is the listed applicant for MMG DISPOSABLE URINARY LEG BAG?

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 DISPOSABLE URINARY LEG BAG?

The FDA product code for MMG DISPOSABLE URINARY LEG BAG is KNX.

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.

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.

View all 11 devices →

Related Devices (Code: KNX)

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.

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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