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FDA 510(k)

TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050

K-Number: K033188 · 2003-11-19

ApplicantIdev Technologies, Inc.
Decision Date2003-11-19
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 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 2003-11-19 under 510(k) number K033188. 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 FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050?

TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 is a medical device that received FDA 510(k) clearance on 2003-11-19. The listed applicant is Idev Technologies, Inc.. The 510(k) number is K033188.

When did TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 receive FDA 510(k) clearance?

TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 received FDA 510(k) clearance on 2003-11-19, under 510(k) number K033188.

Who is the listed applicant for TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050?

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 FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050?

The FDA product code for TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 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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