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FDA 510(k)

THC URINE CALIBRATORS

K-Number: K920749 · 1992-03-18

Decision Date1992-03-18
Product CodeDLJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

THC URINE CALIBRATORS is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Reagents, Inc.. It received FDA 510(k) clearance on 1992-03-18 under 510(k) number K920749. The device is classified under product code DLJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THC URINE CALIBRATORS?

THC URINE CALIBRATORS is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is Diagnostic Reagents, Inc.. The 510(k) number is K920749.

When did THC URINE CALIBRATORS receive FDA 510(k) clearance?

THC URINE CALIBRATORS received FDA 510(k) clearance on 1992-03-18, under 510(k) number K920749.

Who is the listed applicant for THC URINE CALIBRATORS?

The FDA 510(k) record lists Diagnostic Reagents, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THC URINE CALIBRATORS?

The FDA product code for THC URINE CALIBRATORS is DLJ.

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 Diagnostic Reagents, Inc. 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 66 devices →

Related Devices (Code: DLJ)

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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