FDA 510(k)

ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG

K-Number: K823746 · 1983-01-12

Decision Date1983-01-12

Product CodeDIF

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1983-01-12 under 510(k) number K823746. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG?

ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG is a medical device that received FDA 510(k) clearance on 1983-01-12. The listed applicant is Syva Co.. The 510(k) number is K823746.

When did ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG receive FDA 510(k) clearance?

ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG received FDA 510(k) clearance on 1983-01-12, under 510(k) number K823746.

Who is the listed applicant for ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG?

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 ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG?

The FDA product code for ADVANCE SYS. EMIT-AED ANTIEPILEPTIC DRUG is DIF.

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Other records listing Syva Co. as applicant

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Related Devices (Code: DIF)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.