XTEND CIRCUITS (TM)
K-Number: K924627 · 1993-04-07
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Device Summary
Frequently Asked Questions
What is the XTEND CIRCUITS (TM)?
XTEND CIRCUITS (TM) is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Arc Medical, Inc.. The 510(k) number is K924627.
When did XTEND CIRCUITS (TM) receive FDA 510(k) clearance?
XTEND CIRCUITS (TM) received FDA 510(k) clearance on 1993-04-07, under 510(k) number K924627.
Who is the listed applicant for XTEND CIRCUITS (TM)?
The FDA 510(k) record lists Arc Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XTEND CIRCUITS (TM)?
The FDA product code for XTEND CIRCUITS (TM) is CAI.
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 Arc Medical, 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: CAI)
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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