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FDA 510(k)

ADX AMPHETAMINE/METHAMPHEAMINE

K-Number: K890692 · 1989-08-25

ApplicantAbbott Laboratories
Decision Date1989-08-25
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ADX AMPHETAMINE/METHAMPHEAMINE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1989-08-25 under 510(k) number K890692. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADX AMPHETAMINE/METHAMPHEAMINE?

ADX AMPHETAMINE/METHAMPHEAMINE is a medical device that received FDA 510(k) clearance on 1989-08-25. The listed applicant is Abbott Laboratories. The 510(k) number is K890692.

When did ADX AMPHETAMINE/METHAMPHEAMINE receive FDA 510(k) clearance?

ADX AMPHETAMINE/METHAMPHEAMINE received FDA 510(k) clearance on 1989-08-25, under 510(k) number K890692.

Who is the listed applicant for ADX AMPHETAMINE/METHAMPHEAMINE?

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 ADX AMPHETAMINE/METHAMPHEAMINE?

The FDA product code for ADX AMPHETAMINE/METHAMPHEAMINE is DKZ.

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Related Devices (Code: DKZ)

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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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