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

FILAO NC RX PTCA DILATATION CATHETER

K Number: K141933 · Decision Jun 28, 2015
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
85
Applicant Total
11
Review Days
347

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Basic Information

Device Name
FILAO NC RX PTCA DILATATION CATHETER
K Number
K141933
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5100
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Natec Medical , Ltd.
Date Received
July 16, 2014
Decision Date
June 28, 2015
Product Code
LOX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

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Other Clearances by Natec Medical , Ltd.

K Number Device Name
K251915 Amethyst HP PTA OTW 0.035 Catheter
K241040 Amethyst HP PTA OTW 0.035 Catheter
K220410 Ebony HP PTA OTW 0.035 Catheter
K210012 Tamarin Blue PTCA RX Dilatation Catheter
K143041 Ebony PTA 0.014'' over the wire Catheter and Ebony PTA 0.018 over the wire Catheter
K143036 Ebony PTA 0.035 Peripheral Dilatation Catheter
K142459 Ebony PTA 0.014 RX Peripheral Dilatation Catheter
K112735 TAMARIN BLUE PTCA RX DILATATION CATHETER
K112513 EBONY PTA 0.014 PERIPHERAL DILATATION CATHETER
K103354 EBONY PTA .035 PERIPHERAL DILATATION CATHETER
Search all 11 clearances from Natec Medical , Ltd. →