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FDA 510(k)

MMG MULTI LUMON EXTENSION SET

K-Number: K963112 · 1996-11-08

Decision Date1996-11-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MMG MULTI LUMON EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Mmg Healthcare, Inc.. It received FDA 510(k) clearance on 1996-11-08 under 510(k) number K963112. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMG MULTI LUMON EXTENSION SET?

MMG MULTI LUMON EXTENSION SET is a medical device that received FDA 510(k) clearance on 1996-11-08. The listed applicant is Mmg Healthcare, Inc.. The 510(k) number is K963112.

When did MMG MULTI LUMON EXTENSION SET receive FDA 510(k) clearance?

MMG MULTI LUMON EXTENSION SET received FDA 510(k) clearance on 1996-11-08, under 510(k) number K963112.

Who is the listed applicant for MMG MULTI LUMON EXTENSION SET?

The FDA 510(k) record lists Mmg Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MMG MULTI LUMON EXTENSION SET?

The FDA product code for MMG MULTI LUMON EXTENSION SET is FPA.

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.

Related Devices (Code: FPA)

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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