General Procedural Stretchers (P880- P886)
FDA 510(k) K922809 · Hill-Rom, Inc.
510(k) numberK922809
Submission
- Device name
- General Procedural Stretchers (P880- P886)
- Applicant
- Hill-Rom, Inc.
Batesville, TN, US - Received
- June 10, 1992
- Decision date
- March 31, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FPO – Stretcher, Wheeled
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.6910
- Specialty
- General Hospital
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| K112502 | Procedural Strecher with Intellidrive P8000INK · Traditional | 09/19/2011SE |
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Questions and answers
When was General Procedural Stretchers (P880- P886) cleared by the FDA?
General Procedural Stretchers (P880- P886) (K922809) received a 510(k) decision of Substantially Equivalent on March 31, 1993, 294 days after the submission was received.
What is the product code of K922809?
The FDA product code is FPO – Stretcher, Wheeled, a Class II (moderate risk) device regulated under 21 CFR 880.6910.