FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Invacare Platinum 5NXG Oxygen Concentrator
K Number: K203210
·
Decision Apr 12, 2021
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
20
Review Days
164
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Basic Information
- Device Name
- Invacare Platinum 5NXG Oxygen Concentrator
- K Number
- K203210
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5440
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Invacare Corporation
- Date Received
- October 30, 2020
- Decision Date
- April 12, 2021
- Product Code
- CAW
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CAW | Generator, Oxygen, Portable | FDA class 2 | Anesthesiology |
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