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FDA 510(k)

BLOOD UREA NITROGEN BUN

K-Number: K771830 · 1977-10-25

Decision Date1977-10-25
Product CodeCDW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD UREA NITROGEN BUN is the device name listed in this FDA 510(k) record. The listed applicant is Gamma Enterprises, Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771830. 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 BLOOD UREA NITROGEN BUN?

BLOOD UREA NITROGEN BUN is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Gamma Enterprises, Inc.. The 510(k) number is K771830.

When did BLOOD UREA NITROGEN BUN receive FDA 510(k) clearance?

BLOOD UREA NITROGEN BUN received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771830.

Who is the listed applicant for BLOOD UREA NITROGEN BUN?

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

What is the FDA product code for BLOOD UREA NITROGEN BUN?

The FDA product code for BLOOD UREA NITROGEN BUN 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 Gamma Enterprises, 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 23 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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