FDA 510(k)

MENTOR SINGLE COIL URINARY DIVERSION STENT SET

K-Number: K860055 · 1986-03-11

Decision Date1986-03-11

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MENTOR SINGLE COIL URINARY DIVERSION STENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1986-03-11 under 510(k) number K860055. 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 MENTOR SINGLE COIL URINARY DIVERSION STENT SET?

MENTOR SINGLE COIL URINARY DIVERSION STENT SET is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Mentor Corp.. The 510(k) number is K860055.

When did MENTOR SINGLE COIL URINARY DIVERSION STENT SET receive FDA 510(k) clearance?

MENTOR SINGLE COIL URINARY DIVERSION STENT SET received FDA 510(k) clearance on 1986-03-11, under 510(k) number K860055.

Who is the listed applicant for MENTOR SINGLE COIL URINARY DIVERSION STENT SET?

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

What is the FDA product code for MENTOR SINGLE COIL URINARY DIVERSION STENT SET?

The FDA product code for MENTOR SINGLE COIL URINARY DIVERSION STENT SET is FAD.

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Other records listing Mentor Corp. as applicant

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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.