Frova Intubating Introducer

FDA 510(k) K171917 · Cook Incorporated

Substantially Equivalent

510(k) numberK171917

Submission

Device name
Frova Intubating Introducer
Applicant
Cook Incorporated
Bloomington, IN, US
Received
June 27, 2017
Decision date
April 23, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTR – Tube, Tracheal (W/Wo Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5730
Specialty
Anesthesiology
Life-sustaining
Yes

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Questions and answers

When was Frova Intubating Introducer cleared by the FDA?

Frova Intubating Introducer (K171917) received a 510(k) decision of Substantially Equivalent on April 23, 2018, 300 days after the submission was received.

What is the product code of K171917?

The FDA product code is BTR – Tube, Tracheal (W/Wo Connector), a Class II (moderate risk) device regulated under 21 CFR 868.5730.