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FDA 510(k)

GLASSMAN STONE EXTRACTION SET

K-Number: K904472 · 1990-12-28

ApplicantWilson-Cook Medical, Inc.
Decision Date1990-12-28
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GLASSMAN STONE EXTRACTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 1990-12-28 under 510(k) number K904472. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLASSMAN STONE EXTRACTION SET?

GLASSMAN STONE EXTRACTION SET is a medical device that received FDA 510(k) clearance on 1990-12-28. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K904472.

When did GLASSMAN STONE EXTRACTION SET receive FDA 510(k) clearance?

GLASSMAN STONE EXTRACTION SET received FDA 510(k) clearance on 1990-12-28, under 510(k) number K904472.

Who is the listed applicant for GLASSMAN STONE EXTRACTION SET?

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

What is the FDA product code for GLASSMAN STONE EXTRACTION SET?

The FDA product code for GLASSMAN STONE EXTRACTION SET is LQR.

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Related Devices (Code: LQR)

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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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