Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WILSON-COOK COLON DECOMPRESSION SET

K-Number: K900035 · 1990-03-07

Decision Date1990-03-07
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK COLON DECOMPRESSION 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 1990-03-07 under 510(k) number K900035. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK COLON DECOMPRESSION SET?

WILSON-COOK COLON DECOMPRESSION SET is a medical device that received FDA 510(k) clearance on 1990-03-07. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K900035.

When did WILSON-COOK COLON DECOMPRESSION SET receive FDA 510(k) clearance?

WILSON-COOK COLON DECOMPRESSION SET received FDA 510(k) clearance on 1990-03-07, under 510(k) number K900035.

Who is the listed applicant for WILSON-COOK COLON DECOMPRESSION 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 WILSON-COOK COLON DECOMPRESSION SET?

The FDA product code for WILSON-COOK COLON DECOMPRESSION SET is FEG.

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: FEG)

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.

↑