Medical Depot-Wheelchairs, Model Sentra,Astaire and Viper
FDA 510(k) K003783 · Medical Depot, Inc.
510(k) numberK003783
Submission
- Device name
- Medical Depot-Wheelchairs, Model Sentra,Astaire and Viper
- Applicant
- Medical Depot, Inc.
New Port Riche, FL, US - Received
- December 7, 2000
- Decision date
- January 12, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- IOR – Wheelchair, Mechanical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3850
- Specialty
- Physical Medicine
A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets mobility to persons restricted to a sitting position to mean the device type is intended to provide mobility to individuals who have mobility impairments and/or require an assistive device for mobility.
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|---|---|---|---|
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| K260642 | Manual Wheelchair (LW01108)IOR · Traditional | Anhui Longway Medical Technology Co., Ltd. | 06/02/2026SE |
| K260295 | Helio Kids; Apex PIOR · Traditional | Motion Composites | 05/28/2026SE |
| K254141 | Manual Wheelchair (DY01903(2))IOR · Traditional | Guangdong Dayang Medical Technology Co., Ltd. | 05/21/2026SE |
| K260121 | Manual Wheelchair (7101L, 7102LHD)IOR · Traditional | Foshan Nanhai Hongchen Medical Equipment Co., Ltd. | 04/28/2026SE |
| K260319 | K5 wheelchair (16 with swing-away footrest 18 with swing-away footrest 20 with…IOR · Traditional | Zhenjiang Assure Medical Equipment Co., Ltd. | 03/31/2026SE |
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Questions and answers
When was Medical Depot-Wheelchairs, Model Sentra,Astaire and Viper cleared by the FDA?
Medical Depot-Wheelchairs, Model Sentra,Astaire and Viper (K003783) received a 510(k) decision of Substantially Equivalent on January 12, 2001, 36 days after the submission was received.
What is the product code of K003783?
The FDA product code is IOR – Wheelchair, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3850.