FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OXLIFE EXCELL OXYGEN CONCENTRATORS
K Number: K971964
·
Decision Aug 15, 1997
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
273
Applicant Total
3
Review Days
79
Basic Information
- Device Name
- OXLIFE EXCELL OXYGEN CONCENTRATORS
- K Number
- K971964
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5440
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- OXLIFE, INC.
- Date Received
- May 28, 1997
- Decision Date
- August 15, 1997
- 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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