FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
KENT CAMERA
K Number: K113507
·
Decision Aug 8, 2012
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
73
Applicant Total
4
Review Days
254
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Basic Information
- Device Name
- KENT CAMERA
- K Number
- K113507
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2700
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Kent Imaging, Inc.
- Date Received
- November 28, 2011
- Decision Date
- August 8, 2012
- 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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