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FDA 510(k)

IPC-BOOT

K-Number: K070324 · 2007-05-03

ApplicantC-Boot , Ltd.
Decision Date2007-05-03
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IPC-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 2007-05-03 under 510(k) number K070324. 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 IPC-BOOT?

IPC-BOOT is a medical device that received FDA 510(k) clearance on 2007-05-03. The listed applicant is C-Boot , Ltd.. The 510(k) number is K070324.

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

IPC-BOOT received FDA 510(k) clearance on 2007-05-03, under 510(k) number K070324.

Who is the listed applicant for IPC-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 IPC-BOOT?

The FDA product code for IPC-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.

K041659C-BOOT

Related Devices (Code: JOW)

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.

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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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