MINNIE SUPPORT CATHETER
K-Number: K082337 · 2009-01-15
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Device Summary
Frequently Asked Questions
What is the MINNIE SUPPORT CATHETER?
MINNIE SUPPORT CATHETER is a medical device that received FDA 510(k) clearance on 2009-01-15. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K082337.
When did MINNIE SUPPORT CATHETER receive FDA 510(k) clearance?
MINNIE SUPPORT CATHETER received FDA 510(k) clearance on 2009-01-15, under 510(k) number K082337.
Who is the listed applicant for MINNIE SUPPORT CATHETER?
The FDA 510(k) record lists Vascular Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINNIE SUPPORT CATHETER?
The FDA product code for MINNIE SUPPORT CATHETER is DQY.
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 Vascular Solutions, 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: DQY)
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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