FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN
K Number: K131023
·
Decision Oct 11, 2013
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
70
Applicant Total
1
Review Days
182
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Basic Information
- Device Name
- THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN
- K Number
- K131023
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5905
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Medical Products, LLC
- Date Received
- April 12, 2013
- Decision Date
- October 11, 2013
- Product Code
- NFB
- Advisory Committee
- Anesthesiology
- 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 |
|---|---|---|---|
| NFB | Conserver, Oxygen | FDA class 2 | Anesthesiology |
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