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FDA 510(k)

Barone Jejunostomy Catheter Set

K-Number: K160567 · 2017-05-18

Decision Date2017-05-18
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Barone Jejunostomy Catheter Set is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2017-05-18 under approval number K160567. 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 Barone Jejunostomy Catheter Set?

Barone Jejunostomy Catheter Set is a medical device that received FDA 510(k) clearance on 2017-05-18. It is manufactured by Cook Incorporated. The 510(k) number is K160567.

When was Barone Jejunostomy Catheter Set approved by the FDA?

Barone Jejunostomy Catheter Set received FDA 510(k) clearance on 2017-05-18, under approval number K160567.

What company makes Barone Jejunostomy Catheter Set?

Barone Jejunostomy Catheter Set is manufactured by Cook Incorporated.

What is the FDA product code for Barone Jejunostomy Catheter Set?

The FDA product code for Barone Jejunostomy Catheter Set 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.