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FDA 510(k)

EUROCHIMA UREA NITROGEN

K-Number: K810261 · 1981-02-10

Decision Date1981-02-10
Product CodeCDL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EUROCHIMA UREA NITROGEN is the device name listed in this FDA 510(k) record. The listed applicant is Volu Sol Medical Industries. It received FDA 510(k) clearance on 1981-02-10 under 510(k) number K810261. The device is classified under product code CDL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EUROCHIMA UREA NITROGEN?

EUROCHIMA UREA NITROGEN is a medical device that received FDA 510(k) clearance on 1981-02-10. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K810261.

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

EUROCHIMA UREA NITROGEN received FDA 510(k) clearance on 1981-02-10, under 510(k) number K810261.

Who is the listed applicant for EUROCHIMA UREA NITROGEN?

The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUROCHIMA UREA NITROGEN?

The FDA product code for EUROCHIMA UREA NITROGEN is CDL.

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 Volu Sol Medical Industries 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: CDL)

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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