HotDog Warming Mattress + Return Electrode
FDA 510(k) K210727 · Augustine Temperature Management, LLC
510(k) numberK210727
Submission
- Device name
- HotDog Warming Mattress + Return Electrode
- Applicant
- Augustine Temperature Management, LLC
Minneapolis, MN, US - Received
- March 11, 2021
- Decision date
- February 1, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Abbreviated 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GEI – Electrosurgical, Cutting & Coagulation & Accessories
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Specialty
- General, Plastic Surgery
Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
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|---|---|---|
| K232627 | HotDog Warming Mattress + Return ElectrodeDWJ · Special | 04/18/2024SE |
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| K220941 | HotDog Temperature Management SystemDWJ · Traditional | 09/23/2022SE |
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Questions and answers
When was HotDog Warming Mattress + Return Electrode cleared by the FDA?
HotDog Warming Mattress + Return Electrode (K210727) received a 510(k) decision of Substantially Equivalent on February 1, 2022, 327 days after the submission was received.
What is the product code of K210727?
The FDA product code is GEI – Electrosurgical, Cutting & Coagulation & Accessories, a Class II (moderate risk) device regulated under 21 CFR 878.4400.