FDA 510(k)

TDX BENZODIAZEPINES SERUM

K-Number: K883730 · 1988-11-29

Decision Date1988-11-29

Product CodeJXM

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

TDX BENZODIAZEPINES SERUM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-11-29 under 510(k) number K883730. 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 TDX BENZODIAZEPINES SERUM?

TDX BENZODIAZEPINES SERUM is a medical device that received FDA 510(k) clearance on 1988-11-29. The listed applicant is Abbott Laboratories. The 510(k) number is K883730.

When did TDX BENZODIAZEPINES SERUM receive FDA 510(k) clearance?

TDX BENZODIAZEPINES SERUM received FDA 510(k) clearance on 1988-11-29, under 510(k) number K883730.

Who is the listed applicant for TDX BENZODIAZEPINES SERUM?

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 TDX BENZODIAZEPINES SERUM?

The FDA product code for TDX BENZODIAZEPINES SERUM is JXM.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.