GEM FLOW COUPLER DEVICE AND SYSTEM
K-Number: K093310 · 2010-02-01
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Device Summary
Frequently Asked Questions
What is the GEM FLOW COUPLER DEVICE AND SYSTEM?
GEM FLOW COUPLER DEVICE AND SYSTEM is a medical device that received FDA 510(k) clearance on 2010-02-01. The listed applicant is Synovis Micro Companies Alliance, Inc.. The 510(k) number is K093310.
When did GEM FLOW COUPLER DEVICE AND SYSTEM receive FDA 510(k) clearance?
GEM FLOW COUPLER DEVICE AND SYSTEM received FDA 510(k) clearance on 2010-02-01, under 510(k) number K093310.
Who is the listed applicant for GEM FLOW COUPLER DEVICE AND SYSTEM?
The FDA 510(k) record lists Synovis Micro Companies Alliance, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GEM FLOW COUPLER DEVICE AND SYSTEM?
The FDA product code for GEM FLOW COUPLER DEVICE AND SYSTEM is MVR.
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 Synovis Micro Companies Alliance, Inc. 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.
Related Devices (Code: MVR)
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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