TELEMED ERCP CANNULA
K-Number: K901431 · 1990-06-18
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Device Summary
Frequently Asked Questions
What is the TELEMED ERCP CANNULA?
TELEMED ERCP CANNULA is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Telemed Systems, Inc.. The 510(k) number is K901431.
When did TELEMED ERCP CANNULA receive FDA 510(k) clearance?
TELEMED ERCP CANNULA received FDA 510(k) clearance on 1990-06-18, under 510(k) number K901431.
Who is the listed applicant for TELEMED ERCP CANNULA?
The FDA 510(k) record lists Telemed Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TELEMED ERCP CANNULA?
The FDA product code for TELEMED 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 Telemed Systems, 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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