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

ENDOBIONICS MICROSYRINGE (USYRINGE) INFUSION CATHETER

K Number: K040139 · Decision Feb 18, 2004
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
174
Applicant Total
1
Review Days
27

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
ENDOBIONICS MICROSYRINGE (USYRINGE) INFUSION CATHETER
K Number
K040139
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endobionics, Inc.
Date Received
January 22, 2004
Decision Date
February 18, 2004
Product Code
KRA
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
KRA Catheter, Continuous Flush

Similar 510(k) Clearances

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

View all