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FDA 510(k)

BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC

K-Number: K896744 · 1990-02-23

ApplicantBio-Rad
Decision Date1990-02-23
Product CodeJXM
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1990-02-23 under 510(k) number K896744. 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 BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC?

BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC is a medical device that received FDA 510(k) clearance on 1990-02-23. The listed applicant is Bio-Rad. The 510(k) number is K896744.

When did BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC receive FDA 510(k) clearance?

BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC received FDA 510(k) clearance on 1990-02-23, under 510(k) number K896744.

Who is the listed applicant for BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC?

The FDA product code for BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC 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.

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