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

NEPHROSOL

K Number: K822244 · Decision Sep 2, 1982
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
181
Applicant Total
2
Review Days
37

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Basic Information

Device Name
NEPHROSOL
K Number
K822244
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Dialysis Systems, Inc.
Date Received
July 27, 1982
Decision Date
September 2, 1982
Product Code
KOC
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
KOC Accessories, Blood Circuit, Hemodialysis

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Other Clearances by Dialysis Systems, Inc.

K Number Device Name
K030366 BICARD MIXING SYSTEM