FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT

K Number: K161141 · Decision Mar 22, 2017
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
32
Applicant Total
3
Review Days
334

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Basic Information

Device Name
ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT
K Number
K161141
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pentaferte Italia S.R.L.
Date Received
April 22, 2016
Decision Date
March 22, 2017
Product Code
PNR
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
PNR Enteral Syringes With Enteral Specific Connectors

Similar 510(k) Clearances

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

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Other Clearances by Pentaferte Italia S.R.L.

K Number Device Name
K214080 Pentaflush
K211661 ENFit enteral syringes (NUTRIFIT)