Hyper-K Heat System
FDA 510(k) K912722 · Baxter Healthcare Corp
510(k) numberK912722
Submission
- Device name
- Hyper-K Heat System
- Applicant
- Baxter Healthcare Corp
Valencia, CA, US - Received
- June 18, 1991
- Decision date
- September 11, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- ILO – Pack, Hot Or Cold, Water Circulating
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.5720
- Specialty
- Physical Medicine
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Questions and answers
When was Hyper-K Heat System cleared by the FDA?
Hyper-K Heat System (K912722) received a 510(k) decision of Substantially Equivalent on September 11, 1991, 85 days after the submission was received.
What is the product code of K912722?
The FDA product code is ILO – Pack, Hot Or Cold, Water Circulating, a Class II (moderate risk) device regulated under 21 CFR 890.5720.