FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

GlidePath Retro Long-Term Hemodialysis Catheter

K Number: K203575 · Decision Jul 1, 2021
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
123
Applicant Total
31
Review Days
206

Basic Information

Device Name
GlidePath Retro Long-Term Hemodialysis Catheter
K Number
K203575
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
C.R. Bard, Inc.
Date Received
December 7, 2020
Decision Date
July 1, 2021
Product Code
MSD
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
MSD Catheter, Hemodialysis, Implanted

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