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FDA 510(k)

EXCEL STIM II

K-Number: K896908 · 1990-02-20

ApplicantExcel U.S.A.
Decision Date1990-02-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EXCEL STIM II is the device name listed in this FDA 510(k) record. The listed applicant is Excel U.S.A.. It received FDA 510(k) clearance on 1990-02-20 under 510(k) number K896908. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXCEL STIM II?

EXCEL STIM II is a medical device that received FDA 510(k) clearance on 1990-02-20. The listed applicant is Excel U.S.A.. The 510(k) number is K896908.

When did EXCEL STIM II receive FDA 510(k) clearance?

EXCEL STIM II received FDA 510(k) clearance on 1990-02-20, under 510(k) number K896908.

Who is the listed applicant for EXCEL STIM II?

The FDA 510(k) record lists Excel U.S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXCEL STIM II?

The FDA product code for EXCEL STIM II is IPF.

Related Clinical Trials

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.

Other records listing Excel U.S.A. 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.

Related Devices (Code: IPF)

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.

Official Source

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

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