FDA 510(k)

CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT

K-Number: K960148 · 1996-03-25

Decision Date1996-03-25

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1996-03-25 under 510(k) number K960148. 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 CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT?

CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is Cabot Medical Corp.. The 510(k) number is K960148.

When did CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT receive FDA 510(k) clearance?

CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT received FDA 510(k) clearance on 1996-03-25, under 510(k) number K960148.

Who is the listed applicant for CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT?

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

What is the FDA product code for CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT?

The FDA product code for CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT is FAD.

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Related Devices (Code: FAD)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.