EMIT AED CARBAMAZEPINE ASSAY
K-Number: K832720 · 1983-10-04
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Device Summary
Frequently Asked Questions
What is the EMIT AED CARBAMAZEPINE ASSAY?
EMIT AED CARBAMAZEPINE ASSAY is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Syva Co.. The 510(k) number is K832720.
When did EMIT AED CARBAMAZEPINE ASSAY receive FDA 510(k) clearance?
EMIT AED CARBAMAZEPINE ASSAY received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832720.
Who is the listed applicant for EMIT AED CARBAMAZEPINE 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 AED CARBAMAZEPINE ASSAY?
The FDA product code for EMIT AED CARBAMAZEPINE ASSAY is KLT.
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: KLT)
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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