Saratoga SCT Heated Humidification System

FDA 510(k) K854363 · Saratoga Medical Instrumentation, Inc.

Substantially Equivalent

510(k) numberK854363

Submission

Device name
Saratoga SCT Heated Humidification System
Applicant
Saratoga Medical Instrumentation, Inc.
Hadley, NY, US
Received
October 29, 1985
Decision date
December 31, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K251419Laboratorios Biogalenic Sterile Water for Inhalation, USPBTT · Traditional Laboratorios Biogalenic S.A. DE C.V.01/14/2026SE
K253479Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)BTT · Special Fisher & Paykel Healthcare, Ltd.12/19/2025SE
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 Saratoga SCT Heated Humidification System cleared by the FDA?

Saratoga SCT Heated Humidification System (K854363) received a 510(k) decision of Substantially Equivalent on December 31, 1985, 63 days after the submission was received.

What is the product code of K854363?

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