ERCP CANNULA
K-Number: K905714 · 1991-02-01
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Device Summary
Frequently Asked Questions
What is the ERCP CANNULA?
ERCP CANNULA is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is Everest Medical Corp.. The 510(k) number is K905714.
When did ERCP CANNULA receive FDA 510(k) clearance?
ERCP CANNULA received FDA 510(k) clearance on 1991-02-01, under 510(k) number K905714.
Who is the listed applicant for ERCP CANNULA?
The FDA 510(k) record lists Everest Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ERCP CANNULA?
The FDA product code for ERCP CANNULA 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 Everest Medical 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: 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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