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FDA 510(k)

HMT ENDOSCREEN, MODEL ESC 501

K-Number: K942155 · 1994-07-01

ApplicantServicetrends, Inc.
Decision Date1994-07-01
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HMT ENDOSCREEN, MODEL ESC 501 is the device name listed in this FDA 510(k) record. The listed applicant is Servicetrends, Inc.. It received FDA 510(k) clearance on 1994-07-01 under 510(k) number K942155. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HMT ENDOSCREEN, MODEL ESC 501?

HMT ENDOSCREEN, MODEL ESC 501 is a medical device that received FDA 510(k) clearance on 1994-07-01. The listed applicant is Servicetrends, Inc.. The 510(k) number is K942155.

When did HMT ENDOSCREEN, MODEL ESC 501 receive FDA 510(k) clearance?

HMT ENDOSCREEN, MODEL ESC 501 received FDA 510(k) clearance on 1994-07-01, under 510(k) number K942155.

Who is the listed applicant for HMT ENDOSCREEN, MODEL ESC 501?

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 HMT ENDOSCREEN, MODEL ESC 501?

The FDA product code for HMT ENDOSCREEN, MODEL ESC 501 is FCW.

Related Clinical Trials

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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.

K941013HMT ALEXCOPEK940461ALEXANTRIPTOR

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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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