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

Power Acute Triple Lumen Hemodialysis Catheter

K Number: K222170 · Decision Jan 13, 2023
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
11
Applicant Total
11
Review Days
176

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Basic Information

Device Name
Power Acute Triple Lumen Hemodialysis Catheter
K Number
K222170
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Health Line International Corporation
Date Received
July 21, 2022
Decision Date
January 13, 2023
Product Code
NIE
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
NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NIE), ordered by most recent decision date.

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Other Clearances by Health Line International Corporation

K Number Device Name
K200426 Acute Dual Lumen Hemodialysis Catheter
K200263 Health Line CT Midline Catheter
K192533 Health Line CT CVC
K160448 ARTLINE
K140270 NEXUS MIDLINE CT CATHETER
K130851 CASCADE HEMODIALYSIS/APHERESIS CATHETER
K130034 UNI-PICC
K120548 HLIC NEEDLE-LESS VALVE
K101329 SYNERGY CT PICC
K060352 HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS
Search all 11 clearances from Health Line International Corporation →