EMIT-QUINIDINE CONTROL
K-Number: K790402 · 1979-03-15
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Device Summary
Frequently Asked Questions
What is the EMIT-QUINIDINE CONTROL?
EMIT-QUINIDINE CONTROL is a medical device that received FDA 510(k) clearance on 1979-03-15. The listed applicant is Syva Co.. The 510(k) number is K790402.
When did EMIT-QUINIDINE CONTROL receive FDA 510(k) clearance?
EMIT-QUINIDINE CONTROL received FDA 510(k) clearance on 1979-03-15, under 510(k) number K790402.
Who is the listed applicant for EMIT-QUINIDINE CONTROL?
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-QUINIDINE CONTROL?
The FDA product code for EMIT-QUINIDINE CONTROL is LAS.
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: LAS)
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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