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FDA 510(k)

TI2200 TRANSILLUMINATION CABLE

K-Number: K071429 · 2007-09-10

ApplicantKerr Corporation
Decision Date2007-09-10
Product CodeNTK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TI2200 TRANSILLUMINATION CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2007-09-10 under 510(k) number K071429. The device is classified under product code NTK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TI2200 TRANSILLUMINATION CABLE?

TI2200 TRANSILLUMINATION CABLE is a medical device that received FDA 510(k) clearance on 2007-09-10. The listed applicant is Kerr Corporation. The 510(k) number is K071429.

When did TI2200 TRANSILLUMINATION CABLE receive FDA 510(k) clearance?

TI2200 TRANSILLUMINATION CABLE received FDA 510(k) clearance on 2007-09-10, under 510(k) number K071429.

Who is the listed applicant for TI2200 TRANSILLUMINATION CABLE?

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 TI2200 TRANSILLUMINATION CABLE?

The FDA product code for TI2200 TRANSILLUMINATION CABLE is NTK.

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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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