Thermo-Flow Set
FDA 510(k) K914686 · Inhalation Plastics
510(k) numberK914686
Submission
- Device name
- Thermo-Flow Set
- Applicant
- Inhalation Plastics
Chicago, IL, US - Received
- October 18, 1991
- Decision date
- April 15, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262268 | Optiflow Oxygen Kit (AA484J)BTT · Special | Fisher and Paykel Healthcare Limited | 08/27/2026SE |
| K254078 | HVT 2.0BTT · Traditional | Vapotherm, Inc. | 04/13/2026SE |
| K251448 | FL-10000U Respiratory HumidifierBTT · Traditional | Flexicare Medical Limited. | 01/16/2026SE |
| K251419 | Laboratorios Biogalenic Sterile Water for Inhalation, USPBTT · Traditional | Laboratorios Biogalenic S.A. DE C.V. | 01/14/2026SE |
| K253479 | Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)BTT · Special | Fisher & Paykel Healthcare, Ltd. | 12/19/2025SE |
| K250312 | Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus…BTT · Traditional | Medline Industries, LP | 07/02/2025SE |
| K251611 | Optiflow+ Nasal Cannula - Small (OPT942); Optiflow+ Nasal Cannula - Medium (OPT944)…BTT · Special | Fisher & Paykel Healthcare, Ltd. | 06/25/2025SE |
| K242717 | Laboratorios Biogalenic Sterile Water for Inhalation, USPBTT · Traditional | Laboratorios Biogalenic S.A. DE C.V. | 01/30/2025SE |
| K241778 | Hudson RCI Comfort Flo® CubCannulaBTT · Traditional | Medline Industries, LP | 12/19/2024SE |
| K240163 | Hudson RCI® Comfort Flo Nasal Cannula; Hudson RCI® Comfort Flo Plus CannulaBTT · Traditional | Medline Industries, LP | 09/27/2024SE |
More from Medline Industries, LP
| 510(k) | Device | Decision |
|---|---|---|
| K945565 | Spiro-FlexCAI · Traditional | 01/13/1995SE |
| K901315 | Aeromist II NebulizerCAF · Traditional | 09/10/1990SE |
| K900990 | Filt-R-All Bacterial/Viral FilterCAH · Traditional | 04/19/1990SE |
| K900594 | Anesthesia Breathing CircuitCAI · Traditional | 03/15/1990SE |
| K896832 | Filt-R-All Bacterial FilterCAH · Traditional | 01/22/1990SE |
| K874659 | Sterilization of Devices by RadiationBTT · Traditional | 02/02/1988SE |
Questions and answers
When was Thermo-Flow Set cleared by the FDA?
Thermo-Flow Set (K914686) received a 510(k) decision of Substantially Equivalent on April 15, 1992, 180 days after the submission was received.
What is the product code of K914686?
The FDA product code is BTT – Humidifier, Respiratory Gas, (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5450.