ACE CONNECT INTERNAL CONNECTION
K-Number: K041759 · 2004-07-22
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Device Summary
Frequently Asked Questions
What is the ACE CONNECT INTERNAL CONNECTION?
ACE CONNECT INTERNAL CONNECTION is a medical device that received FDA 510(k) clearance on 2004-07-22. The listed applicant is Ace Surgical Supply Co., Inc.. The 510(k) number is K041759.
When did ACE CONNECT INTERNAL CONNECTION receive FDA 510(k) clearance?
ACE CONNECT INTERNAL CONNECTION received FDA 510(k) clearance on 2004-07-22, under 510(k) number K041759.
Who is the listed applicant for ACE CONNECT INTERNAL CONNECTION?
The FDA 510(k) record lists Ace Surgical Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACE CONNECT INTERNAL CONNECTION?
The FDA product code for ACE CONNECT INTERNAL CONNECTION is DZE.
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 Ace Surgical Supply Co., 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: DZE)
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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