OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO
K-Number: K851647 · 1985-07-03
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Device Summary
Frequently Asked Questions
What is the OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO?
OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO is a medical device that received FDA 510(k) clearance on 1985-07-03. The listed applicant is Meadox Surgimed, Inc.. The 510(k) number is K851647.
When did OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO receive FDA 510(k) clearance?
OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO received FDA 510(k) clearance on 1985-07-03, under 510(k) number K851647.
Who is the listed applicant for OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO?
The FDA 510(k) record lists Meadox Surgimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO?
The FDA product code for OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO 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 Meadox Surgimed, 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.
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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