EMIT QST PHENOBARBITAL ASSAY
K-Number: K834216 · 1984-01-24
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Device Summary
Frequently Asked Questions
What is the EMIT QST PHENOBARBITAL ASSAY?
EMIT QST PHENOBARBITAL ASSAY is a medical device that received FDA 510(k) clearance on 1984-01-24. The listed applicant is Syva Co.. The 510(k) number is K834216.
When did EMIT QST PHENOBARBITAL ASSAY receive FDA 510(k) clearance?
EMIT QST PHENOBARBITAL ASSAY received FDA 510(k) clearance on 1984-01-24, under 510(k) number K834216.
Who is the listed applicant for EMIT QST PHENOBARBITAL ASSAY?
The FDA 510(k) record lists Syva Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMIT QST PHENOBARBITAL ASSAY?
The FDA product code for EMIT QST PHENOBARBITAL ASSAY is DLZ.
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 Syva Co. 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: DLZ)
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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