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FDA 510(k)

TDX CANNABINOIDS-GS

K-Number: K883731 · 1988-10-11

ApplicantAbbott Laboratories
Decision Date1988-10-11
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TDX 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 1988-10-11 under 510(k) number K883731. 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 TDX CANNABINOIDS-GS?

TDX CANNABINOIDS-GS is a medical device that received FDA 510(k) clearance on 1988-10-11. The listed applicant is Abbott Laboratories. The 510(k) number is K883731.

When did TDX CANNABINOIDS-GS receive FDA 510(k) clearance?

TDX CANNABINOIDS-GS received FDA 510(k) clearance on 1988-10-11, under 510(k) number K883731.

Who is the listed applicant for TDX 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 TDX CANNABINOIDS-GS?

The FDA product code for TDX 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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