REUSABLE BRONCHIAL BIOPSY FORCEPS
K-Number: K022398 · 2002-10-11
Advertisement
Device Summary
Frequently Asked Questions
What is the REUSABLE BRONCHIAL BIOPSY FORCEPS?
REUSABLE BRONCHIAL BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Ballard Medical Products. The 510(k) number is K022398.
When did REUSABLE BRONCHIAL BIOPSY FORCEPS receive FDA 510(k) clearance?
REUSABLE BRONCHIAL BIOPSY FORCEPS received FDA 510(k) clearance on 2002-10-11, under 510(k) number K022398.
Who is the listed applicant for REUSABLE BRONCHIAL BIOPSY FORCEPS?
The FDA 510(k) record lists Ballard Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REUSABLE BRONCHIAL BIOPSY FORCEPS?
The FDA product code for REUSABLE BRONCHIAL BIOPSY FORCEPS is BWH.
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 Ballard Medical Products 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.
Related Devices (Code: BWH)
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.
Advertisement