FDA 510(k)

REVISIED LABELING FOR ADX BENZODIAZEPINES

K-Number: K880014 · 1988-02-11

Decision Date1988-02-11

Product CodeJXM

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

REVISIED LABELING FOR ADX 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 1988-02-11 under 510(k) number K880014. 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 REVISIED LABELING FOR ADX BENZODIAZEPINES?

REVISIED LABELING FOR ADX BENZODIAZEPINES is a medical device that received FDA 510(k) clearance on 1988-02-11. The listed applicant is Abbott Laboratories. The 510(k) number is K880014.

When did REVISIED LABELING FOR ADX BENZODIAZEPINES receive FDA 510(k) clearance?

REVISIED LABELING FOR ADX BENZODIAZEPINES received FDA 510(k) clearance on 1988-02-11, under 510(k) number K880014.

Who is the listed applicant for REVISIED LABELING FOR ADX 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 REVISIED LABELING FOR ADX BENZODIAZEPINES?

The FDA product code for REVISIED LABELING FOR ADX 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.