FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
CEROX MODEL 3210
K Number: K093923
·
Decision Jan 19, 2010
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
73
Applicant Total
5
Review Days
28
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Basic Information
- Device Name
- CEROX MODEL 3210
- K Number
- K093923
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.2700
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Or-Nim Medical , Ltd.
- Date Received
- December 22, 2009
- Decision Date
- January 19, 2010
- Product Code
- MUD
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| MUD | Oximeter, Tissue Saturation | FDA class 2 | Cardiovascular |
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