GT LEGGIERO
K-Number: K981359 · 1999-01-27
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Device Summary
Frequently Asked Questions
What is the GT LEGGIERO?
GT LEGGIERO is a medical device that received FDA 510(k) clearance on 1999-01-27. The listed applicant is Terumo Medical Corp.. The 510(k) number is K981359.
When did GT LEGGIERO receive FDA 510(k) clearance?
GT LEGGIERO received FDA 510(k) clearance on 1999-01-27, under 510(k) number K981359.
Who is the listed applicant for GT LEGGIERO?
The FDA 510(k) record lists Terumo Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GT LEGGIERO?
The FDA product code for GT LEGGIERO is DQY.
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 Terumo Medical Corp. 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: DQY)
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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