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FDA 510(k)

IMMULITE CANNABINOIDS

K-Number: K963916 · 1997-04-28

Decision Date1997-04-28
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

IMMULITE CANNABINOIDS is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1997-04-28 under 510(k) number K963916. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMULITE CANNABINOIDS?

IMMULITE CANNABINOIDS is a medical device that received FDA 510(k) clearance on 1997-04-28. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K963916.

When did IMMULITE CANNABINOIDS receive FDA 510(k) clearance?

IMMULITE CANNABINOIDS received FDA 510(k) clearance on 1997-04-28, under 510(k) number K963916.

Who is the listed applicant for IMMULITE CANNABINOIDS?

The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMMULITE CANNABINOIDS?

The FDA product code for IMMULITE CANNABINOIDS 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 Diagnostic Products Corp. 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.

View all 321 devices →

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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