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FDA 510(k)

TDXR DELTA-9-CANNABINOIDS

K-Number: K874646 · 1987-12-18

ApplicantAbbott Laboratories
Decision Date1987-12-18
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TDXR DELTA-9-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 1987-12-18 under 510(k) number K874646. 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 TDXR DELTA-9-CANNABINOIDS?

TDXR DELTA-9-CANNABINOIDS is a medical device that received FDA 510(k) clearance on 1987-12-18. The listed applicant is Abbott Laboratories. The 510(k) number is K874646.

When did TDXR DELTA-9-CANNABINOIDS receive FDA 510(k) clearance?

TDXR DELTA-9-CANNABINOIDS received FDA 510(k) clearance on 1987-12-18, under 510(k) number K874646.

Who is the listed applicant for TDXR DELTA-9-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 TDXR DELTA-9-CANNABINOIDS?

The FDA product code for TDXR DELTA-9-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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