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FDA 510(k)

Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED

K-Number: K821950 · 1982-07-20

Decision Date1982-07-20
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1982-07-20 under 510(k) number K821950. 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 Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED?

Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K821950.

When did Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED receive FDA 510(k) clearance?

Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821950.

Who is the listed applicant for Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED?

The FDA product code for Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED 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 Travenol Laboratories, S.A. 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 206 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

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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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