AMERICAN CATHETER E.R.C.P. CANNULA
K-Number: K940370 · 1994-08-17
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Device Summary
Frequently Asked Questions
What is the AMERICAN CATHETER E.R.C.P. CANNULA?
AMERICAN CATHETER E.R.C.P. CANNULA is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Intl. Medical, Inc.. The 510(k) number is K940370.
When did AMERICAN CATHETER E.R.C.P. CANNULA receive FDA 510(k) clearance?
AMERICAN CATHETER E.R.C.P. CANNULA received FDA 510(k) clearance on 1994-08-17, under 510(k) number K940370.
Who is the listed applicant for AMERICAN CATHETER E.R.C.P. CANNULA?
The FDA 510(k) record lists Intl. Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMERICAN CATHETER E.R.C.P. CANNULA?
The FDA product code for AMERICAN CATHETER E.R.C.P. 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 Intl. Medical, 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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