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FDA 510(k)

CANNABINOIDS

K-Number: K013247 · 2002-03-13

ApplicantAbbott Laboratories
Decision Date2002-03-13
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CANNABINOIDS is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2002-03-13 under 510(k) number K013247. 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 CANNABINOIDS?

CANNABINOIDS is a medical device that received FDA 510(k) clearance on 2002-03-13. The listed applicant is Abbott Laboratories. The 510(k) number is K013247.

When did CANNABINOIDS receive FDA 510(k) clearance?

CANNABINOIDS received FDA 510(k) clearance on 2002-03-13, under 510(k) number K013247.

Who is the listed applicant for CANNABINOIDS?

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

What is the FDA product code for CANNABINOIDS?

The FDA product code for CANNABINOIDS is LDJ.

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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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