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FDA 510(k)

4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS

K-Number: K933109 · 1994-03-28

ApplicantBoston Pacific Medical, Inc.
Decision Date1994-03-28
Product CodeKOD
Advisory CommitteeGU
DecisionUnknown

Device Summary

4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Boston Pacific Medical, Inc.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K933109. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the 4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS?

4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Boston Pacific Medical, Inc.. The 510(k) number is K933109.

When did 4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS receive FDA 510(k) clearance?

4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS received FDA 510(k) clearance on 1994-03-28, under 510(k) number K933109.

Who is the listed applicant for 4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS?

The FDA 510(k) record lists Boston Pacific Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS?

The FDA product code for 4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS is KOD.

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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.

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