FDA 510(k)

TSC

K-Number: K101756 · 2010-10-26

Decision Date2010-10-26

Product CodeMVL

DecisionSubstantially Equivalent

Device Summary

TSC is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2010-10-26 under 510(k) number K101756. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TSC?

TSC is a medical device that received FDA 510(k) clearance on 2010-10-26. The listed applicant is Kerr Corporation. The 510(k) number is K101756.

When did TSC receive FDA 510(k) clearance?

TSC received FDA 510(k) clearance on 2010-10-26, under 510(k) number K101756.

Who is the listed applicant for TSC?

The FDA 510(k) record lists Kerr Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TSC?

The FDA product code for TSC is MVL.

Other records listing Kerr Corporation 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.

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Related Devices (Code: MVL)

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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.