Restcue CC
FDA 510(k) K922973 · Support Systems Intl.
510(k) numberK922973
Submission
- Device name
- Restcue CC
- Applicant
- Support Systems Intl.
Charleston, SC, US - Received
- June 22, 1992
- Decision date
- July 30, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- IOQ – Bed, Flotation Therapy, Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.5170
- Specialty
- Physical Medicine
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Questions and answers
When was Restcue CC cleared by the FDA?
Restcue CC (K922973) received a 510(k) decision of Substantially Equivalent on July 30, 1992, 38 days after the submission was received.
What is the product code of K922973?
The FDA product code is IOQ – Bed, Flotation Therapy, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5170.