Merits E700 Porce Lift
FDA 510(k) K073513 · Merits Health Products Co., Ltd.
510(k) numberK073513
Submission
- Device name
- Merits E700 Porce Lift
- Applicant
- Merits Health Products Co., Ltd.
Taichung, TW - Received
- December 14, 2007
- Decision date
- January 14, 2008
- Decision
- Substantially Equivalent (SESE)
- Type
- Abbreviated 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- ING – Elevator, Wheelchair, Portable
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.3930
- Specialty
- Physical Medicine
A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs).
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Questions and answers
When was Merits E700 Porce Lift cleared by the FDA?
Merits E700 Porce Lift (K073513) received a 510(k) decision of Substantially Equivalent on January 14, 2008, 31 days after the submission was received.
What is the product code of K073513?
The FDA product code is ING – Elevator, Wheelchair, Portable, a Class II (moderate risk) device regulated under 21 CFR 890.3930.