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FDA 510(k)

DE-TOX TUBES A AND DE-TOX TUBES B

K-Number: K904326 · 1991-01-17

Decision Date1991-01-17
Product CodeDPA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DE-TOX TUBES A AND DE-TOX TUBES B is the device name listed in this FDA 510(k) record. The listed applicant is Dyna-Tek Industries. It received FDA 510(k) clearance on 1991-01-17 under 510(k) number K904326. The device is classified under product code DPA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DE-TOX TUBES A AND DE-TOX TUBES B?

DE-TOX TUBES A AND DE-TOX TUBES B is a medical device that received FDA 510(k) clearance on 1991-01-17. The listed applicant is Dyna-Tek Industries. The 510(k) number is K904326.

When did DE-TOX TUBES A AND DE-TOX TUBES B receive FDA 510(k) clearance?

DE-TOX TUBES A AND DE-TOX TUBES B received FDA 510(k) clearance on 1991-01-17, under 510(k) number K904326.

Who is the listed applicant for DE-TOX TUBES A AND DE-TOX TUBES B?

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

What is the FDA product code for DE-TOX TUBES A AND DE-TOX TUBES B?

The FDA product code for DE-TOX TUBES A AND DE-TOX TUBES B is DPA.

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 Dyna-Tek Industries 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.

Related Devices (Code: DPA)

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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