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
PIF Gastrointestinal Tubes With Enteral Specific Connectors

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PIF), ordered by most recent decision date.

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Other Clearances by Rockfield Medical

K Number Device Name
K233034 Mobility+ Enteral Feeding System OTC