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FDA 510(k)

URETERAL CATHETER AND ACCESSORIES

K-Number: K934419 · 1994-05-25

ApplicantUrological Associates of Central Jersey P.A.
Decision Date1994-05-25
Product CodeEYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URETERAL CATHETER AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Urological Associates of Central Jersey P.A.. It received FDA 510(k) clearance on 1994-05-25 under 510(k) number K934419. The device is classified under product code EYK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URETERAL CATHETER AND ACCESSORIES?

URETERAL CATHETER AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-05-25. The listed applicant is Urological Associates of Central Jersey P.A.. The 510(k) number is K934419.

When did URETERAL CATHETER AND ACCESSORIES receive FDA 510(k) clearance?

URETERAL CATHETER AND ACCESSORIES received FDA 510(k) clearance on 1994-05-25, under 510(k) number K934419.

Who is the listed applicant for URETERAL CATHETER AND ACCESSORIES?

The FDA 510(k) record lists Urological Associates of Central Jersey P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URETERAL CATHETER AND ACCESSORIES?

The FDA product code for URETERAL CATHETER AND ACCESSORIES is EYK.

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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.

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