FDA 510(k)

ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT

K-Number: K864225 · 1987-01-30

Decision Date1987-01-30

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT is the device name listed in this FDA 510(k) record. The listed applicant is Angiomed U.S., Inc.. It received FDA 510(k) clearance on 1987-01-30 under 510(k) number K864225. 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 ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT?

ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT is a medical device that received FDA 510(k) clearance on 1987-01-30. The listed applicant is Angiomed U.S., Inc.. The 510(k) number is K864225.

When did ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT receive FDA 510(k) clearance?

ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT received FDA 510(k) clearance on 1987-01-30, under 510(k) number K864225.

Who is the listed applicant for ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT?

The FDA 510(k) record lists Angiomed U.S., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT?

The FDA product code for ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID 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.