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FDA 510(k)

LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS

K-Number: K904541 · 1990-11-20

ApplicantAbbott Laboratories
Decision Date1990-11-20
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1990-11-20 under 510(k) number K904541. 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 LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS?

LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS is a medical device that received FDA 510(k) clearance on 1990-11-20. The listed applicant is Abbott Laboratories. The 510(k) number is K904541.

When did LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS receive FDA 510(k) clearance?

LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS received FDA 510(k) clearance on 1990-11-20, under 510(k) number K904541.

Who is the listed applicant for LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS?

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 LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS?

The FDA product code for LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS 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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