EXCEL STIM II
K-Number: K896908 · 1990-02-20
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Device Summary
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
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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