FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REDSENSE-HOME USE
K Number: K092955
·
Decision May 10, 2010
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
3
Applicant Total
4
Review Days
227
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Basic Information
- Device Name
- REDSENSE-HOME USE
- K Number
- K092955
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5820
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Redsense Medical AB
- Date Received
- September 25, 2009
- Decision Date
- May 10, 2010
- Product Code
- ODX
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| ODX | Autonomous Extracorporeal Blood Leak Detector/Alarm | FDA class 2 | Gastroenterology, Urology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (ODX), ordered by most recent decision date.
REDSENSE ALARM SYSTEM
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REDSENSE
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