FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EMPTY EVA SOLUTION CONTAINER EMPTY EVA DUAL CHAMBER SOLUTION CONTAINER

K Number: K121161 · Decision Jul 13, 2012
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
3
Review Days
87

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Basic Information

Device Name
EMPTY EVA SOLUTION CONTAINER EMPTY EVA DUAL CHAMBER SOLUTION CONTAINER
K Number
K121161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acta Medical, LLC
Date Received
April 17, 2012
Decision Date
July 13, 2012
Product Code
KPE
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPE Container, I.V.

Similar 510(k) Clearances

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

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Other Clearances by Acta Medical, LLC

K Number Device Name
K121803 INTRAVASCULAR ADMINISTRATION SET
K112863 ENTERAL ADMINISTRATION SET WITH SOLUTION CONTAINER, ENTERAL ADMINISTRATION SET, ENTERAL EXTENSION SET WITH MINITUBE CONN