CONTROL SET, EMIT METHOTREXATE
K-Number: K781827 · 1979-01-03
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Device Summary
Frequently Asked Questions
What is the CONTROL SET, EMIT METHOTREXATE?
CONTROL SET, EMIT METHOTREXATE is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is Syva Co.. The 510(k) number is K781827.
When did CONTROL SET, EMIT METHOTREXATE receive FDA 510(k) clearance?
CONTROL SET, EMIT METHOTREXATE received FDA 510(k) clearance on 1979-01-03, under 510(k) number K781827.
Who is the listed applicant for CONTROL SET, EMIT METHOTREXATE?
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 CONTROL SET, EMIT METHOTREXATE?
The FDA product code for CONTROL SET, EMIT METHOTREXATE 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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