FLEX-NECK ARC CATHETER
K-Number: K070730 · 2007-07-03
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Device Summary
Frequently Asked Questions
What is the FLEX-NECK ARC CATHETER?
FLEX-NECK ARC CATHETER is a medical device that received FDA 510(k) clearance on 2007-07-03. The listed applicant is Medigroup, Inc.. The 510(k) number is K070730.
When did FLEX-NECK ARC CATHETER receive FDA 510(k) clearance?
FLEX-NECK ARC CATHETER received FDA 510(k) clearance on 2007-07-03, under 510(k) number K070730.
Who is the listed applicant for FLEX-NECK ARC CATHETER?
The FDA 510(k) record lists Medigroup, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEX-NECK ARC CATHETER?
The FDA product code for FLEX-NECK ARC CATHETER is FJS.
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 Medigroup, 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: FJS)
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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