INTRASTENT
K-Number: K991929 · 1999-08-04
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Device Summary
Frequently Asked Questions
What is the INTRASTENT?
INTRASTENT is a medical device that received FDA 510(k) clearance on 1999-08-04. The listed applicant is Intratherapeutics, Inc.. The 510(k) number is K991929.
When did INTRASTENT receive FDA 510(k) clearance?
INTRASTENT received FDA 510(k) clearance on 1999-08-04, under 510(k) number K991929.
Who is the listed applicant for INTRASTENT?
The FDA 510(k) record lists Intratherapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRASTENT?
The FDA product code for INTRASTENT is FGE.
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 Intratherapeutics, 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.
Related Devices (Code: FGE)
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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