FDA 510(k)

MESH URETERAL STENT

K-Number: K011264 · 2001-07-17

ApplicantApplied Medical Resources Corp.

Decision Date2001-07-17

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MESH URETERAL STENT is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2001-07-17 under 510(k) number K011264. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MESH URETERAL STENT?

MESH URETERAL STENT is a medical device that received FDA 510(k) clearance on 2001-07-17. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K011264.

When did MESH URETERAL STENT receive FDA 510(k) clearance?

MESH URETERAL STENT received FDA 510(k) clearance on 2001-07-17, under 510(k) number K011264.

Who is the listed applicant for MESH URETERAL STENT?

The FDA 510(k) record lists Applied Medical Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MESH URETERAL STENT?

The FDA product code for MESH URETERAL STENT is FAD.

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Related Devices (Code: FAD)

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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.