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FDA 510(k)

SOEHENDRA LITHOTRIPSY SET

K-Number: K902170 · 1990-07-25

Decision Date1990-07-25
Product CodeLQC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SOEHENDRA LITHOTRIPSY 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 1990-07-25 under 510(k) number K902170. The device is classified under product code LQC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOEHENDRA LITHOTRIPSY SET?

SOEHENDRA LITHOTRIPSY SET is a medical device that received FDA 510(k) clearance on 1990-07-25. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K902170.

When did SOEHENDRA LITHOTRIPSY SET receive FDA 510(k) clearance?

SOEHENDRA LITHOTRIPSY SET received FDA 510(k) clearance on 1990-07-25, under 510(k) number K902170.

Who is the listed applicant for SOEHENDRA LITHOTRIPSY 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 SOEHENDRA LITHOTRIPSY SET?

The FDA product code for SOEHENDRA LITHOTRIPSY SET is LQC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Wilson-Cook Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 122 devices →

Related Devices (Code: LQC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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