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 a medical device manufactured by D4D Technologies, LLC. It received FDA 510(k) clearance on 2022-04-29 under approval 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. It is manufactured by D4D Technologies, LLC. The 510(k) number is K213482.
When was TIA Tip, Cariosity, Transillumination Accessory Tip approved by the FDA?
TIA Tip, Cariosity, Transillumination Accessory Tip received FDA 510(k) clearance on 2022-04-29, under approval number K213482.
What company makes TIA Tip, Cariosity, Transillumination Accessory Tip?
TIA Tip, Cariosity, Transillumination Accessory Tip is manufactured by D4D Technologies, LLC.
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)
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.