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

DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)

K Number: K020430 · Decision May 9, 2002
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
15
Review Days
90

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)
K Number
K020430
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diatek, Inc.
Date Received
February 8, 2002
Decision Date
May 9, 2002
Product Code
NFK
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
NFK Kit, Repair, Catheter, Hemodialysis

Similar 510(k) Clearances

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

View all

Other Clearances by Diatek, Inc.

K Number Device Name
K010399 DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)
K895703 DIATEK MODEL 700 THERMOMETER
K872178 MODIFICATION TO ARKIVE(TM)
K862085 ARKIVE (TM)
K841827 ENTEROPORT NUTRITION PUMP
K841859 SECURA SET
K833568 DIATEK 600 THERMOMETER SYSTEM
K830565 SECURA SET SECONDARY ADMIN. SET
K830377 SECURA SET PRIMARY ADMIN. SET
K830355 SECURA IV VOLUMETRIC INFUSION PUMP
Search all 15 clearances from Diatek, Inc. →