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FDA 510(k)

Safety Trocar Cannula

K-Number: K211072 · 2021-04-27

Decision Date2021-04-27
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Safety Trocar Cannula is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2021-04-27 under approval number K211072. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Safety Trocar Cannula?

Safety Trocar Cannula is a medical device that received FDA 510(k) clearance on 2021-04-27. It is manufactured by Boston Scientific Corporation. The 510(k) number is K211072.

When was Safety Trocar Cannula approved by the FDA?

Safety Trocar Cannula received FDA 510(k) clearance on 2021-04-27, under approval number K211072.

What company makes Safety Trocar Cannula?

Safety Trocar Cannula is manufactured by Boston Scientific Corporation.

What is the FDA product code for Safety Trocar Cannula?

The FDA product code for Safety Trocar Cannula is KNT.

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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.