URETERAL DILATION SET
K-Number: K832808 · 1983-10-14
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Device Summary
Frequently Asked Questions
What is the URETERAL DILATION SET?
URETERAL DILATION SET is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Van-Tec, Inc.. The 510(k) number is K832808.
When did URETERAL DILATION SET receive FDA 510(k) clearance?
URETERAL DILATION SET received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832808.
Who is the listed applicant for URETERAL DILATION 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 DILATION SET?
The FDA product code for URETERAL DILATION SET is EZN.
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: EZN)
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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