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 BRONCHOSCOPE BIOPSY FORCEPS

K-Number: K901348 · 1990-10-09

Decision Date1990-10-09
Product CodeEGQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS 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 1990-10-09 under 510(k) number K901348. The device is classified under product code EGQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS?

WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K901348.

When did WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS receive FDA 510(k) clearance?

WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS received FDA 510(k) clearance on 1990-10-09, under 510(k) number K901348.

Who is the listed applicant for WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS?

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 BRONCHOSCOPE BIOPSY FORCEPS?

The FDA product code for WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS is EGQ.

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 →

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.

↑