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

DAYTON WATER SYSTEMS ULTRAPURE WATER TREATMENT SYSTEMS FOR HEMODIALYSIS

K Number: K021352 · Decision Aug 1, 2002
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
3
Review Days
94

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DAYTON WATER SYSTEMS ULTRAPURE WATER TREATMENT SYSTEMS FOR HEMODIALYSIS
K Number
K021352
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dayton Water Systems
Date Received
April 29, 2002
Decision Date
August 1, 2002
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 Dayton Water Systems

K Number Device Name
K981680 ULTRAPURE WATER TREATMENT SYSTEM FOR HEMODIALYSIS
K924695 ASEPTECH PORTABLE RO+ SYSTEM