FDA 510(k)

C-BOOT

K-Number: K041659 · 2004-10-28

Decision Date2004-10-28

Product CodeJOW

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

C-BOOT is the device name listed in this FDA 510(k) record. The listed applicant is C-Boot , Ltd.. It received FDA 510(k) clearance on 2004-10-28 under 510(k) number K041659. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C-BOOT?

C-BOOT is a medical device that received FDA 510(k) clearance on 2004-10-28. The listed applicant is C-Boot , Ltd.. The 510(k) number is K041659.

When did C-BOOT receive FDA 510(k) clearance?

C-BOOT received FDA 510(k) clearance on 2004-10-28, under 510(k) number K041659.

Who is the listed applicant for C-BOOT?

The FDA 510(k) record lists C-Boot , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C-BOOT?

The FDA product code for C-BOOT is JOW.

Other records listing C-Boot , Ltd. 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.

K070324IPC-BOOT

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.