FDA.reportPublic FDA data

510(k) K050926

Device
TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060
Applicant
Idev Technologies, Inc.
510(k) number
K050926
Product code
MMX
Decision
Substantially Equivalent (SESE)
Decision date
2005-05-09
Date received
2005-04-13
Regulation
870.5150
Classification name
Device, Percutaneous Retrieval
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
SHANNON HURD
Address
1110 Nasa Rd. One Suite 311 Houston TX US 77058 77058

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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