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

TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060

K Number: K050926 · Decision May 9, 2005
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
31
Applicant Total
11
Review Days
26

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Basic Information

Device Name
TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060
K Number
K050926
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Idev Technologies, Inc.
Date Received
April 13, 2005
Decision Date
May 9, 2005
Product Code
MMX
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
MMX Device, Percutaneous Retrieval

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Other Clearances by Idev Technologies, Inc.

K Number Device Name
K130591 SUPERA VERITAS
K122546 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
K111627 SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
K111766 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS
K093893 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
K071646 SUPERA INTERWOVEN SELF-EXPANDING BILIARY NITINOL STENT DELIVERY CATHETER, MODEL # S-04-040-120
K060557 SURESAVE TM SELF-EXPANDABLE NITINOL STENT AND PRECISION TM DELIVERY CATHETER-SS06120060
K041374 AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060
K033188 TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050
K030504 AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060
Search all 11 clearances from Idev Technologies, Inc. →