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FDA 510(k)

BENZODIAZEPINES BY REMEDI HS

K-Number: K955116 · 1996-01-30

ApplicantBio-Rad
Decision Date1996-01-30
Product CodeLAA
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

BENZODIAZEPINES BY REMEDI HS is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1996-01-30 under 510(k) number K955116. The device is classified under product code LAA. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENZODIAZEPINES BY REMEDI HS?

BENZODIAZEPINES BY REMEDI HS is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Bio-Rad. The 510(k) number is K955116.

When did BENZODIAZEPINES BY REMEDI HS receive FDA 510(k) clearance?

BENZODIAZEPINES BY REMEDI HS received FDA 510(k) clearance on 1996-01-30, under 510(k) number K955116.

Who is the listed applicant for BENZODIAZEPINES BY REMEDI HS?

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 BY REMEDI HS?

The FDA product code for BENZODIAZEPINES BY REMEDI HS is LAA.

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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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