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FDA 510(k)

TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060

K-Number: K050926 · 2005-05-09

ApplicantIdev Technologies, Inc.
Decision Date2005-05-09
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 is the device name listed in this FDA 510(k) record. The listed applicant is Idev Technologies, Inc.. It received FDA 510(k) clearance on 2005-05-09 under 510(k) number K050926. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060?

TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 is a medical device that received FDA 510(k) clearance on 2005-05-09. The listed applicant is Idev Technologies, Inc.. The 510(k) number is K050926.

When did TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 receive FDA 510(k) clearance?

TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 received FDA 510(k) clearance on 2005-05-09, under 510(k) number K050926.

Who is the listed applicant for TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060?

The FDA 510(k) record lists Idev Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060?

The FDA product code for TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 is MMX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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