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

AquaA

K Number: K252181 · Decision Sep 9, 2025
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
42
Review Days
60

Basic Information

Device Name
AquaA
K Number
K252181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fresenius Medical Care North America
Date Received
July 11, 2025
Decision Date
September 9, 2025
Product Code
FIP
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
FIP Subsystem, Water Purification

Similar 510(k) Clearances

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

View all

Other Clearances by Fresenius Medical Care North America

K Number Device Name
K162488 Optiflux dialyzer
K152953 CRIT-LINE CLIP (CLIC) BLOOD CHAMBER
K152367 Optiflux dialyzer
K123262 OPTIFLUX ULTRA DIALYZER
K131611 FRESENIUS DRY ACID DISSOLUTION UNITS
K124035 2008K@HOME HEMODIALYSIS MACHINE
K121341 FRESENIUS 2008T HEMODIALYSIS MACHINE WITH BIBAG SYSTEM
K120017 FRESENIUS 2008 HEMODIAYSIS MACHINE WITH BIBAG SYSTEM
K113427 FRESENIUS 2008T HEMODIALYSIS MACHINE
K070049 FRESENIUS 2008K @HOME WITH WIRELESS WETNESS DETECTOR
Search all 42 clearances from Fresenius Medical Care North America →