FDA 510(k)

ADX TM BENZODIAZEPINES

K-Number: K890691 · 1989-08-25

Decision Date1989-08-25

Product CodeJXM

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

ADX TM BENZODIAZEPINES 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 K890691. The device is classified under product code JXM. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADX TM BENZODIAZEPINES?

ADX TM BENZODIAZEPINES 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 K890691.

When did ADX TM BENZODIAZEPINES receive FDA 510(k) clearance?

ADX TM BENZODIAZEPINES received FDA 510(k) clearance on 1989-08-25, under 510(k) number K890691.

Who is the listed applicant for ADX TM BENZODIAZEPINES?

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 TM BENZODIAZEPINES?

The FDA product code for ADX TM BENZODIAZEPINES is JXM.

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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.