SECURA SET
K-Number: K841859 · 1984-07-03
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Device Summary
Frequently Asked Questions
What is the SECURA SET?
SECURA SET is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is Diatek, Inc.. The 510(k) number is K841859.
When did SECURA SET receive FDA 510(k) clearance?
SECURA SET received FDA 510(k) clearance on 1984-07-03, under 510(k) number K841859.
Who is the listed applicant for SECURA SET?
The FDA 510(k) record lists Diatek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SECURA SET?
The FDA product code for SECURA SET is FPA.
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 Diatek, 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: FPA)
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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