RK2000 K-Thermia System
FDA 510(k) K882442 · Baxter Healthcare Corp
510(k) numberK882442
Submission
- Device name
- RK2000 K-Thermia System
- Applicant
- Baxter Healthcare Corp
Valencia, CA, US - Received
- June 14, 1988
- Decision date
- September 6, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DWJ – System, Thermal Regulating
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5900
- Specialty
- Cardiovascular
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
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Questions and answers
When was RK2000 K-Thermia System cleared by the FDA?
RK2000 K-Thermia System (K882442) received a 510(k) decision of Substantially Equivalent on September 6, 1988, 84 days after the submission was received.
What is the product code of K882442?
The FDA product code is DWJ – System, Thermal Regulating, a Class II (moderate risk) device regulated under 21 CFR 870.5900.