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

PEREGRINE SYSTEM INFUSION CATHETER

K Number: K140637 · Decision Mar 26, 2014
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
174
Applicant Total
2
Review Days
14

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Basic Information

Device Name
PEREGRINE SYSTEM INFUSION CATHETER
K Number
K140637
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ablative Solutions, Inc.
Date Received
March 12, 2014
Decision Date
March 26, 2014
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.

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Other Clearances by Ablative Solutions, Inc.

K Number Device Name
K231279 Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mm