WANG BRONCHIAL NEEDLE BRUSH
K-Number: K944650 · 1994-11-22
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Device Summary
Frequently Asked Questions
What is the WANG BRONCHIAL NEEDLE BRUSH?
WANG BRONCHIAL NEEDLE BRUSH is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K944650.
When did WANG BRONCHIAL NEEDLE BRUSH receive FDA 510(k) clearance?
WANG BRONCHIAL NEEDLE BRUSH received FDA 510(k) clearance on 1994-11-22, under 510(k) number K944650.
Who is the listed applicant for WANG BRONCHIAL NEEDLE BRUSH?
The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WANG BRONCHIAL NEEDLE BRUSH?
The FDA product code for WANG BRONCHIAL NEEDLE BRUSH is EOQ.
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 Mill-Rose Laboratory 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: EOQ)
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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