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FDA 510(k)

EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010

K-Number: K874477 · 1987-11-23

Decision Date1987-11-23
Product CodeCDQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010 is the device name listed in this FDA 510(k) record. The listed applicant is Em Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K874477. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010?

EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010 is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K874477.

When did EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010 receive FDA 510(k) clearance?

EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010 received FDA 510(k) clearance on 1987-11-23, under 510(k) number K874477.

Who is the listed applicant for EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010?

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

What is the FDA product code for EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010?

The FDA product code for EASY-TEST UREA NITROGEN (BUN) ITEM NUMBER: 19010 is CDQ.

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 Em Diagnostic Systems, 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 288 devices →

Related Devices (Code: CDQ)

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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