A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD
K-Number: K850032 · 1985-02-01
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Device Summary
Frequently Asked Questions
What is the A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD?
A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD is a medical device that received FDA 510(k) clearance on 1985-02-01. The listed applicant is Paco Research Corp.. The 510(k) number is K850032.
When did A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD receive FDA 510(k) clearance?
A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD received FDA 510(k) clearance on 1985-02-01, under 510(k) number K850032.
Who is the listed applicant for A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD?
The FDA 510(k) record lists Paco Research Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD?
The FDA product code for A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD is BSY.
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 Paco Research Corp. 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: BSY)
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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