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FDA 510(k)

ALEXANTRIPTOR

K-Number: K940461 · 1994-06-02

ApplicantServicetrends, Inc.
Decision Date1994-06-02
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALEXANTRIPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Servicetrends, Inc.. It received FDA 510(k) clearance on 1994-06-02 under 510(k) number K940461. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALEXANTRIPTOR?

ALEXANTRIPTOR is a medical device that received FDA 510(k) clearance on 1994-06-02. The listed applicant is Servicetrends, Inc.. The 510(k) number is K940461.

When did ALEXANTRIPTOR receive FDA 510(k) clearance?

ALEXANTRIPTOR received FDA 510(k) clearance on 1994-06-02, under 510(k) number K940461.

Who is the listed applicant for ALEXANTRIPTOR?

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

What is the FDA product code for ALEXANTRIPTOR?

The FDA product code for ALEXANTRIPTOR is GEX. This falls under the Gastroenterology category.

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Other records listing Servicetrends, Inc. as applicant

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

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