FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ReddyPort NIV Access Elbow
K Number: K171827
·
Decision Jan 19, 2018
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
46
Applicant Total
2
Review Days
213
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Basic Information
- Device Name
- ReddyPort NIV Access Elbow
- K Number
- K171827
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5895
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Smd Manufacturing, LLC
- Date Received
- June 20, 2017
- Decision Date
- January 19, 2018
- Product Code
- MNS
- 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 |
|---|---|---|---|
| MNS | Ventilator, Continuous, Non-Life-Supporting | FDA class 2 | Anesthesiology |
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Other Clearances by Smd Manufacturing, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K231064 | ReddyPort Elbow | Jul 13, 2023 | Substantially Equivalent |