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FDA 510(k)

URISTOP

K-Number: K803109 · 1981-02-25

ApplicantThe Sora Co.
Decision Date1981-02-25
Product Code
DecisionSubstantially Equivalent

Device Summary

URISTOP is the device name listed in this FDA 510(k) record. The listed applicant is The Sora Co.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K803109. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URISTOP?

URISTOP is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is The Sora Co.. The 510(k) number is K803109.

When did URISTOP receive FDA 510(k) clearance?

URISTOP received FDA 510(k) clearance on 1981-02-25, under 510(k) number K803109.

Who is the listed applicant for URISTOP?

The FDA 510(k) record lists The Sora Co. as the applicant. This does not by itself establish the device manufacturer.

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.

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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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