CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT
K-Number: K921464 · 1992-05-05
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Device Summary
Frequently Asked Questions
What is the CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT?
CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT is a medical device that received FDA 510(k) clearance on 1992-05-05. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K921464.
When did CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT receive FDA 510(k) clearance?
CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT received FDA 510(k) clearance on 1992-05-05, under 510(k) number K921464.
Who is the listed applicant for CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT?
The FDA 510(k) record lists Trinity Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT?
The FDA product code for CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT is GBQ.
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 Trinity Laboratories, 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: GBQ)
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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