EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM
K-Number: K060494 · 2006-07-03
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Device Summary
Frequently Asked Questions
What is the EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM?
EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2006-07-03. The listed applicant is Medchannel, LLC. The 510(k) number is K060494.
When did EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM receive FDA 510(k) clearance?
EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM received FDA 510(k) clearance on 2006-07-03, under 510(k) number K060494.
Who is the listed applicant for EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM?
The FDA 510(k) record lists Medchannel, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM?
The FDA product code for EASYTAC ANCHOR. EASYTAC DELIVERY SYSTEM is GDW.
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 Medchannel, LLC 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: GDW)
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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