PANCREATIC DRAINAGE TUBE
K-Number: K021672 · 2003-04-16
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Device Summary
Frequently Asked Questions
What is the PANCREATIC DRAINAGE TUBE?
PANCREATIC DRAINAGE TUBE is a medical device that received FDA 510(k) clearance on 2003-04-16. The listed applicant is Aomori Olympus Co., Ltd.. The 510(k) number is K021672.
When did PANCREATIC DRAINAGE TUBE receive FDA 510(k) clearance?
PANCREATIC DRAINAGE TUBE received FDA 510(k) clearance on 2003-04-16, under 510(k) number K021672.
Who is the listed applicant for PANCREATIC DRAINAGE TUBE?
The FDA 510(k) record lists Aomori Olympus Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PANCREATIC DRAINAGE TUBE?
The FDA product code for PANCREATIC DRAINAGE TUBE 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 Aomori Olympus Co., Ltd. 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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