FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇪 Ireland
Mobility+ Enteral Feeding System
K Number: K222678
·
Decision Oct 27, 2022
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
49
Applicant Total
2
Review Days
51
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Basic Information
- Device Name
- Mobility+ Enteral Feeding System
- K Number
- K222678
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5980
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Rockfield Medical
- Date Received
- September 6, 2022
- Decision Date
- October 27, 2022
- Product Code
- PIF
- 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 |
|---|---|---|---|
| PIF | Gastrointestinal Tubes With Enteral Specific Connectors | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Rockfield Medical
| K Number | Device Name | ||
|---|---|---|---|
| K233034 | Mobility+ Enteral Feeding System OTC | Apr 12, 2024 | Substantially Equivalent |