SECURA SET SECONDARY ADMIN. SET
K-Number: K830565 · 1983-03-09
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Device Summary
Frequently Asked Questions
What is the SECURA SET SECONDARY ADMIN. SET?
SECURA SET SECONDARY ADMIN. SET is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Diatek, Inc.. The 510(k) number is K830565.
When did SECURA SET SECONDARY ADMIN. SET receive FDA 510(k) clearance?
SECURA SET SECONDARY ADMIN. SET received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830565.
Who is the listed applicant for SECURA SET SECONDARY ADMIN. 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 SECONDARY ADMIN. SET?
The FDA product code for SECURA SET SECONDARY ADMIN. 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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