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

CCPD CYCLER SET

K Number: K810670 · Decision Mar 24, 1981
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
112
Applicant Total
30
Review Days
12

Basic Information

Device Name
CCPD CYCLER SET
K Number
K810670
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Date Received
March 12, 1981
Decision Date
March 24, 1981
Product Code
KDJ
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
KDJ Set, Administration, For Peritoneal Dialysis, Disposable

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