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FDA 510(k)

TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS

K-Number: K873183 · 1987-11-23

Decision Date1987-11-23
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K873183. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS?

TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Abbott Laboratories. The 510(k) number is K873183.

When did TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS receive FDA 510(k) clearance?

TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873183.

Who is the listed applicant for TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS?

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 TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS?

The FDA product code for TDXR MULTICONSTIT. CONTROLS FOR ABUSED DRUG ASSAYS is DIF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Abbott Laboratories as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: DIF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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