BARD-PARKER BILIARY BALLOON CATHETER
K-Number: K852293 · 1985-10-04
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Device Summary
Frequently Asked Questions
What is the BARD-PARKER BILIARY BALLOON CATHETER?
BARD-PARKER BILIARY BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 1985-10-04. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K852293.
When did BARD-PARKER BILIARY BALLOON CATHETER receive FDA 510(k) clearance?
BARD-PARKER BILIARY BALLOON CATHETER received FDA 510(k) clearance on 1985-10-04, under 510(k) number K852293.
Who is the listed applicant for BARD-PARKER BILIARY BALLOON CATHETER?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARD-PARKER BILIARY BALLOON CATHETER?
The FDA product code for BARD-PARKER BILIARY BALLOON CATHETER is FGE.
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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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: FGE)
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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