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FDA 510(k)

MMG CATHETER PLUG W/DRAINAGE TUBE COVER

K-Number: K874682 · 1988-01-27

Decision Date1988-01-27
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MMG CATHETER PLUG W/DRAINAGE TUBE COVER 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 1988-01-27 under 510(k) number K874682. 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 CATHETER PLUG W/DRAINAGE TUBE COVER?

MMG CATHETER PLUG W/DRAINAGE TUBE COVER is a medical device that received FDA 510(k) clearance on 1988-01-27. The listed applicant is Medical Marketing Group. The 510(k) number is K874682.

When did MMG CATHETER PLUG W/DRAINAGE TUBE COVER receive FDA 510(k) clearance?

MMG CATHETER PLUG W/DRAINAGE TUBE COVER received FDA 510(k) clearance on 1988-01-27, under 510(k) number K874682.

Who is the listed applicant for MMG CATHETER PLUG W/DRAINAGE TUBE COVER?

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 CATHETER PLUG W/DRAINAGE TUBE COVER?

The FDA product code for MMG CATHETER PLUG W/DRAINAGE TUBE COVER is KOD.

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: 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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