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

SINGLE-PATIENT AUTOMATIC DIALYSIS UNIT MOD. DBB-22

K Number: K863609 · Decision Feb 25, 1987
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
49
Applicant Total
9
Review Days
162

Basic Information

Device Name
SINGLE-PATIENT AUTOMATIC DIALYSIS UNIT MOD. DBB-22
K Number
K863609
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
INTERNATIONAL MEDICAL PRODUCTS, INC.
Date Received
September 16, 1986
Decision Date
February 25, 1987
Product Code
FKP
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
FKP System, Dialysate Delivery, Single Patient

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