AST INCORPORATING DST
K-Number: K961114 · 1996-05-23
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Device Summary
Frequently Asked Questions
What is the AST INCORPORATING DST?
AST INCORPORATING DST is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is Trace Scientific , Ltd.. The 510(k) number is K961114.
When did AST INCORPORATING DST receive FDA 510(k) clearance?
AST INCORPORATING DST received FDA 510(k) clearance on 1996-05-23, under 510(k) number K961114.
Who is the listed applicant for AST INCORPORATING DST?
The FDA 510(k) record lists Trace Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AST INCORPORATING DST?
The FDA product code for AST INCORPORATING DST is CIT.
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 Trace Scientific , Ltd. 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: CIT)
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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