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FDA 510(k)

TIA Tip, Cariosity, Transillumination Accessory Tip

K-Number: K213482 · 2022-04-29

ApplicantD4D Technologies, LLC
Decision Date2022-04-29
Product CodeNTK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TIA Tip, Cariosity, Transillumination Accessory Tip is the device name listed in this FDA 510(k) record. The listed applicant is D4D Technologies, LLC. It received FDA 510(k) clearance on 2022-04-29 under 510(k) number K213482. 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 TIA Tip, Cariosity, Transillumination Accessory Tip?

TIA Tip, Cariosity, Transillumination Accessory Tip is a medical device that received FDA 510(k) clearance on 2022-04-29. The listed applicant is D4D Technologies, LLC. The 510(k) number is K213482.

When did TIA Tip, Cariosity, Transillumination Accessory Tip receive FDA 510(k) clearance?

TIA Tip, Cariosity, Transillumination Accessory Tip received FDA 510(k) clearance on 2022-04-29, under 510(k) number K213482.

Who is the listed applicant for TIA Tip, Cariosity, Transillumination Accessory Tip?

The FDA 510(k) record lists D4D Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIA Tip, Cariosity, Transillumination Accessory Tip?

The FDA product code for TIA Tip, Cariosity, Transillumination Accessory Tip is NTK.

Related Devices (Code: NTK)

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

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

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