FDA 510(k)

MODIFICATION TO URETERAL STENT

K-Number: K040760 · 2004-10-15

ApplicantApplied Medical Resources Corp.

Decision Date2004-10-15

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO 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 2004-10-15 under 510(k) number K040760. 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 MODIFICATION TO URETERAL STENT?

MODIFICATION TO URETERAL STENT is a medical device that received FDA 510(k) clearance on 2004-10-15. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K040760.

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

MODIFICATION TO URETERAL STENT received FDA 510(k) clearance on 2004-10-15, under 510(k) number K040760.

Who is the listed applicant for MODIFICATION TO 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 MODIFICATION TO URETERAL STENT?

The FDA product code for MODIFICATION TO 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.