CANNABINOID ENZYME IMMUNOASSAY KIT
K-Number: K872882 · 1987-11-03
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Device Summary
Frequently Asked Questions
What is the CANNABINOID ENZYME IMMUNOASSAY KIT?
CANNABINOID ENZYME IMMUNOASSAY KIT is a medical device that received FDA 510(k) clearance on 1987-11-03. The listed applicant is General Diagnostics. The 510(k) number is K872882.
When did CANNABINOID ENZYME IMMUNOASSAY KIT receive FDA 510(k) clearance?
CANNABINOID ENZYME IMMUNOASSAY KIT received FDA 510(k) clearance on 1987-11-03, under 510(k) number K872882.
Who is the listed applicant for CANNABINOID ENZYME IMMUNOASSAY KIT?
The FDA 510(k) record lists General Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CANNABINOID ENZYME IMMUNOASSAY KIT?
The FDA product code for CANNABINOID ENZYME IMMUNOASSAY KIT is LDJ.
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 General Diagnostics 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: LDJ)
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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