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FDA 510(k)

Trapper Exchange Device

K-Number: K162253 · 2017-01-06

ApplicantCreganna Medical Aslo Business AS Cregganna Tactx Medical
Decision Date2017-01-06
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Trapper Exchange Device is a medical device manufactured by Creganna Medical Aslo Business AS Cregganna Tactx Medical. It received FDA 510(k) clearance on 2017-01-06 under approval number K162253. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trapper Exchange Device?

Trapper Exchange Device is a medical device that received FDA 510(k) clearance on 2017-01-06. It is manufactured by Creganna Medical Aslo Business AS Cregganna Tactx Medical. The 510(k) number is K162253.

When was Trapper Exchange Device approved by the FDA?

Trapper Exchange Device received FDA 510(k) clearance on 2017-01-06, under approval number K162253.

What company makes Trapper Exchange Device?

Trapper Exchange Device is manufactured by Creganna Medical Aslo Business AS Cregganna Tactx Medical.

What is the FDA product code for Trapper Exchange Device?

The FDA product code for Trapper Exchange Device is DQY.

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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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