FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PERCUTANEOUS NEPHROSTOMY SET

K Number: K820867 · Decision Apr 13, 1982
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
10
Applicant Total
52
Review Days
15

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Basic Information

Device Name
PERCUTANEOUS NEPHROSTOMY SET
K Number
K820867
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
March 29, 1982
Decision Date
April 13, 1982
Product Code
GBO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GBO Catheter, Nephrostomy, General & Plastic Surgery

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K871777 VAN-TEC REUSABLE HELICAL STONE BASKET
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