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FDA 510(k)

EXCEL TX

K-Number: K940200 · 1994-06-07

ApplicantExcel Tech. , Ltd.
Decision Date1994-06-07
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EXCEL TX is the device name listed in this FDA 510(k) record. The listed applicant is Excel Tech. , Ltd.. It received FDA 510(k) clearance on 1994-06-07 under 510(k) number K940200. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXCEL TX?

EXCEL TX is a medical device that received FDA 510(k) clearance on 1994-06-07. The listed applicant is Excel Tech. , Ltd.. The 510(k) number is K940200.

When did EXCEL TX receive FDA 510(k) clearance?

EXCEL TX received FDA 510(k) clearance on 1994-06-07, under 510(k) number K940200.

Who is the listed applicant for EXCEL TX?

The FDA 510(k) record lists Excel Tech. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXCEL TX?

The FDA product code for EXCEL TX is ITH.

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Related Devices (Code: ITH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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