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FDA 510(k)

THERACHEM TDC THERAPEUTIC DRUG CONTROL

K-Number: K840921 · 1984-04-05

Decision Date1984-04-05
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

THERACHEM TDC THERAPEUTIC DRUG CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Diagnostics. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K840921. 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 THERACHEM TDC THERAPEUTIC DRUG CONTROL?

THERACHEM TDC THERAPEUTIC DRUG CONTROL is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Fisher Diagnostics. The 510(k) number is K840921.

When did THERACHEM TDC THERAPEUTIC DRUG CONTROL receive FDA 510(k) clearance?

THERACHEM TDC THERAPEUTIC DRUG CONTROL received FDA 510(k) clearance on 1984-04-05, under 510(k) number K840921.

Who is the listed applicant for THERACHEM TDC THERAPEUTIC DRUG CONTROL?

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

What is the FDA product code for THERACHEM TDC THERAPEUTIC DRUG CONTROL?

The FDA product code for THERACHEM TDC THERAPEUTIC DRUG CONTROL 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 Fisher Diagnostics 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.

View all 16 devices →

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

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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