Model 720 Series Full/Semi Electric Bed 1120 Full Electric Bed
FDA 510(k) K974296 · Invacare Corp.
510(k) numberK974296
Submission
- Device name
- Model 720 Series Full/Semi Electric Bed 1120 Full Electric Bed
- Applicant
- Invacare Corp.
Elyria, OH, US - Received
- November 17, 1997
- Decision date
- January 6, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FNL – Bed, Ac-Powered Adjustable Hospital
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5100
- Specialty
- General Hospital
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Questions and answers
When was Model 720 Series Full/Semi Electric Bed 1120 Full Electric Bed cleared by the FDA?
Model 720 Series Full/Semi Electric Bed 1120 Full Electric Bed (K974296) received a 510(k) decision of Substantially Equivalent on January 6, 1998, 50 days after the submission was received.
What is the product code of K974296?
The FDA product code is FNL – Bed, Ac-Powered Adjustable Hospital, a Class II (moderate risk) device regulated under 21 CFR 880.5100.