URETERAL STANT SET
K-Number: K820870 · 1982-04-26
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Device Summary
Frequently Asked Questions
What is the URETERAL STANT SET?
URETERAL STANT SET is a medical device that received FDA 510(k) clearance on 1982-04-26. The listed applicant is Van-Tec, Inc.. The 510(k) number is K820870.
When did URETERAL STANT SET receive FDA 510(k) clearance?
URETERAL STANT SET received FDA 510(k) clearance on 1982-04-26, under 510(k) number K820870.
Who is the listed applicant for URETERAL STANT SET?
The FDA 510(k) record lists Van-Tec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URETERAL STANT SET?
The FDA product code for URETERAL STANT SET is FAD.
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 Van-Tec, 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.
Related Devices (Code: FAD)
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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