Goodknight H20, Model M-114600-00
FDA 510(k) K042184 · Mallinckrodt Developpement France
510(k) numberK042184
Submission
- Device name
- Goodknight H20, Model M-114600-00
- Applicant
- Mallinckrodt Developpement France
Villers-Les-Nancy Cedex, FR - Received
- August 12, 2004
- Decision date
- January 10, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
- Third-party review
- Yes
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 |
|---|---|---|
| K082237 | Puritan Bennett, Sandman Duo and Sandman Duo STBZD · Special | 10/09/2008SE |
| K080439 | Sandman Info Without Humidifier/ Sandman Auto Without Humidifier, Model…BZD · Special | 05/16/2008SE |
| K071575 | Sandman IntroBZD · Traditional | 09/10/2007SE |
| K063501 | Knightcontrol Remote Control, Model M-114700-USBZD · Traditional | 04/06/2007SE |
| K041819 | Goodknight 425, MODELM-114500-00BZD · Special | 07/22/2004SE |
| K001845 | Mallinckrodt, Goodknight 418SBZD · Special | 07/05/2000SE |
Questions and answers
When was Goodknight H20, Model M-114600-00 cleared by the FDA?
Goodknight H20, Model M-114600-00 (K042184) received a 510(k) decision of Substantially Equivalent on January 10, 2005, 151 days after the submission was received.
What is the product code of K042184?
The FDA product code is BTT – Humidifier, Respiratory Gas, (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5450.