FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
PHILIPS SPO2 REUSABLE SENSORS, MODEL NOS. M1191T, M1192T, AND M1193T
K Number: K032979
·
Decision Feb 20, 2004
Classifications
1
FEI Numbers
403
Registration Numbers
403
Same Product Code
711
Applicant Total
111
Review Days
149
Basic Information
- Device Name
- PHILIPS SPO2 REUSABLE SENSORS, MODEL NOS. M1191T, M1192T, AND M1193T
- K Number
- K032979
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.2700
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- PHILIPS MEDICAL SYSTEMS, INC.
- Date Received
- September 24, 2003
- Decision Date
- February 20, 2004
- 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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