FDA Registration Active 🇺🇸 United States

GlidePath™ Long Term Hemodialysis Catheter

Reg #: 3006260740 · FEI: 3006260740 · Expires 2025
Products
1
Proprietary Names
3
Establishment Types
1
Classifications
1

Registration Details

Registration Name
Bard Access Systems, Inc.
Registration Number
3006260740
FEI Number
3006260740
Status
Active
Expiry Year
2025
Initial Importer
Yes
Address
605 North 5600 West
City
Salt Lake City
State
UT
ZIP
84116
Country
US

Regulatory Submissions

510(k) Number
K190527

Owner / Operator

Firm Name
C. R. Bard, Inc.
Operator Number
2212754
Address
1 Becton Drive
City
Franklin Lakes
State
NJ
Postal Code
07417
Country
US

Products

Device Name Product Code
Catheter, Hemodialysis, Implanted MSD

Proprietary Names

GlidePath™ Long Term Hemodialysis Catheter HemoStar™ Long Term Hemodialysis Catheter HemoStar XK™ Long Term Hemodialysis Catheter

Establishment Types

Manufacture Medical Device