Salter Labs Bubble Humidifier (High Flow)

FDA 510(k) K113542 · Salter Labs, Arvin Facility

Substantially Equivalent

510(k) numberK113542

Submission

Device name
Salter Labs Bubble Humidifier (High Flow)
Applicant
Salter Labs, Arvin Facility
Arvin, CA, US
Received
December 1, 2011
Decision date
February 10, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
BTT – Humidifier, Respiratory Gas, (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5450
Specialty
Anesthesiology

Other 510(k)s with product code BTT

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K262268Optiflow Oxygen Kit (AA484J)BTT · Special Fisher and Paykel Healthcare Limited08/27/2026SE
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K251448FL-10000U Respiratory HumidifierBTT · Traditional Flexicare Medical Limited.01/16/2026SE
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K250312Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus…BTT · Traditional Medline Industries, LP07/02/2025SE
K251611Optiflow+ Nasal Cannula - Small (OPT942); Optiflow+ Nasal Cannula - Medium (OPT944)…BTT · Special Fisher & Paykel Healthcare, Ltd.06/25/2025SE
K242717Laboratorios Biogalenic Sterile Water for Inhalation, USPBTT · Traditional Laboratorios Biogalenic S.A. DE C.V.01/30/2025SE
K241778Hudson RCI Comfort Flo® CubCannula™BTT · Traditional Medline Industries, LP12/19/2024SE
K240163Hudson RCI® Comfort Flo Nasal Cannula; Hudson RCI® Comfort Flo Plus CannulaBTT · Traditional Medline Industries, LP09/27/2024SE

Questions and answers

When was Salter Labs Bubble Humidifier (High Flow) cleared by the FDA?

Salter Labs Bubble Humidifier (High Flow) (K113542) received a 510(k) decision of Substantially Equivalent on February 10, 2012, 71 days after the submission was received.

What is the product code of K113542?

The FDA product code is BTT – Humidifier, Respiratory Gas, (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5450.