MMG MULTI LUMON EXTENSION SET
K-Number: K963112 · 1996-11-08
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Device Summary
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
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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