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

ACETIC ACID WAND, ACID WAND ASSEMBLY, BICARBONATE WAND ASSEMBLY

K Number: K133299 · Decision Jul 7, 2014
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
336
Applicant Total
1
Review Days
255

Basic Information

Device Name
ACETIC ACID WAND, ACID WAND ASSEMBLY, BICARBONATE WAND ASSEMBLY
K Number
K133299
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
FRESENIUS MEDICAL CARE, NORTH AMERICA - RENAL THER
Date Received
October 25, 2013
Decision Date
July 7, 2014
Product Code
KDI
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
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

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