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FDA 510(k)

UREA NITROGEN REAGENT SET

K-Number: K844156 · 1984-11-13

Decision Date1984-11-13
Product CodeCDW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UREA NITROGEN REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Livonia Diagnostics, Inc.. It received FDA 510(k) clearance on 1984-11-13 under 510(k) number K844156. The device is classified under product code CDW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UREA NITROGEN REAGENT SET?

UREA NITROGEN REAGENT SET is a medical device that received FDA 510(k) clearance on 1984-11-13. The listed applicant is Livonia Diagnostics, Inc.. The 510(k) number is K844156.

When did UREA NITROGEN REAGENT SET receive FDA 510(k) clearance?

UREA NITROGEN REAGENT SET received FDA 510(k) clearance on 1984-11-13, under 510(k) number K844156.

Who is the listed applicant for UREA NITROGEN REAGENT SET?

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

What is the FDA product code for UREA NITROGEN REAGENT SET?

The FDA product code for UREA NITROGEN REAGENT SET is CDW.

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 Livonia Diagnostics, 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 16 devices →

Related Devices (Code: CDW)

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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