Pressure Release Valve W/Audible, Model PRV 20/40/60; with T6 Adapter, Model PRV 120/140/160; T6 Adapter, Model T6-100

FDA 510(k) K091538 · Wet Nose Technologies, LLC

Substantially Equivalent

510(k) numberK091538

Submission

Device name
Pressure Release Valve W/Audible, Model PRV 20/40/60; with T6 Adapter, Model PRV 120/140/160; T6 Adapter, Model T6-100
Applicant
Wet Nose Technologies, LLC
Los Angeles, CA, US
Received
May 26, 2009
Decision date
March 25, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CBP – Valve, Non-Rebreathing
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5870
Specialty
Anesthesiology
Life-sustaining
Yes

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K132143Exhalation ValveCBP · Traditional Intersurgical Incorporated06/04/2014SE

More from Intersurgical Incorporated

510(k)DeviceDecision
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Questions and answers

When was Pressure Release Valve W/Audible, Model PRV 20/40/60; with T6 Adapter, Model PRV 120/140/160; T6 Adapter, Model T6-100 cleared by the FDA?

Pressure Release Valve W/Audible, Model PRV 20/40/60; with T6 Adapter, Model PRV 120/140/160; T6 Adapter, Model T6-100 (K091538) received a 510(k) decision of Substantially Equivalent on March 25, 2010, 303 days after the submission was received.

What is the product code of K091538?

The FDA product code is CBP – Valve, Non-Rebreathing, a Class II (moderate risk) device regulated under 21 CFR 868.5870.