EZ-CONNECT
K-Number: K061771 · 2006-07-10
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Device Summary
Frequently Asked Questions
What is the EZ-CONNECT?
EZ-CONNECT is a medical device that received FDA 510(k) clearance on 2006-07-10. The listed applicant is Vidacare Corporation. The 510(k) number is K061771.
When did EZ-CONNECT receive FDA 510(k) clearance?
EZ-CONNECT received FDA 510(k) clearance on 2006-07-10, under 510(k) number K061771.
Who is the listed applicant for EZ-CONNECT?
The FDA 510(k) record lists Vidacare Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EZ-CONNECT?
The FDA product code for EZ-CONNECT 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.
Other records listing Vidacare Corporation 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: 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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