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FDA 510(k)

DISPOSABLE URINARY LEGBAG W/STRAP

K-Number: K821168 · 1982-05-24

Decision Date1982-05-24
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE URINARY LEGBAG W/STRAP 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 1982-05-24 under 510(k) number K821168. 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 DISPOSABLE URINARY LEGBAG W/STRAP?

DISPOSABLE URINARY LEGBAG W/STRAP is a medical device that received FDA 510(k) clearance on 1982-05-24. The listed applicant is Medical Marketing Group. The 510(k) number is K821168.

When did DISPOSABLE URINARY LEGBAG W/STRAP receive FDA 510(k) clearance?

DISPOSABLE URINARY LEGBAG W/STRAP received FDA 510(k) clearance on 1982-05-24, under 510(k) number K821168.

Who is the listed applicant for DISPOSABLE URINARY LEGBAG W/STRAP?

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 DISPOSABLE URINARY LEGBAG W/STRAP?

The FDA product code for DISPOSABLE URINARY LEGBAG W/STRAP 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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