ORAL THC-CANNABINOIDS DIRECT RIA KIT
K-Number: K843534 · 1984-10-30
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Device Summary
Frequently Asked Questions
What is the ORAL THC-CANNABINOIDS DIRECT RIA KIT?
ORAL THC-CANNABINOIDS DIRECT RIA KIT is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Immunalysis Corporation. The 510(k) number is K843534.
When did ORAL THC-CANNABINOIDS DIRECT RIA KIT receive FDA 510(k) clearance?
ORAL THC-CANNABINOIDS DIRECT RIA KIT received FDA 510(k) clearance on 1984-10-30, under 510(k) number K843534.
Who is the listed applicant for ORAL THC-CANNABINOIDS DIRECT RIA KIT?
The FDA 510(k) record lists Immunalysis Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORAL THC-CANNABINOIDS DIRECT RIA KIT?
The FDA product code for ORAL THC-CANNABINOIDS DIRECT RIA KIT is LAT.
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 Immunalysis Corporation 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: LAT)
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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