SWITCH-IT CATHETER
K-Number: K120707 · 2012-05-15
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Device Summary
Frequently Asked Questions
What is the SWITCH-IT CATHETER?
SWITCH-IT CATHETER is a medical device that received FDA 510(k) clearance on 2012-05-15. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K120707.
When did SWITCH-IT CATHETER receive FDA 510(k) clearance?
SWITCH-IT CATHETER received FDA 510(k) clearance on 2012-05-15, under 510(k) number K120707.
Who is the listed applicant for SWITCH-IT 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 SWITCH-IT CATHETER?
The FDA product code for SWITCH-IT 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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