FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SPO2 FINGER PROBES
K Number: K973970
·
Decision Oct 6, 1998
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
3
Review Days
354
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Basic Information
- Device Name
- SPO2 FINGER PROBES
- K Number
- K973970
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2700
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Medical Cables, Inc.
- Date Received
- October 17, 1997
- Decision Date
- October 6, 1998
- Product Code
- DQA
- Advisory Committee
- Cardiovascular
- 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 |
|---|---|---|---|
| DQA | Oximeter | FDA class 2 | Cardiovascular |
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