FLOW2, SWING
K-Number: K121561 · 2012-10-26
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Device Summary
Frequently Asked Questions
What is the FLOW2, SWING?
FLOW2, SWING is a medical device that received FDA 510(k) clearance on 2012-10-26. The listed applicant is Thyssenkrupp Accessibility B.V.. The 510(k) number is K121561.
When did FLOW2, SWING receive FDA 510(k) clearance?
FLOW2, SWING received FDA 510(k) clearance on 2012-10-26, under 510(k) number K121561.
Who is the listed applicant for FLOW2, SWING?
The FDA 510(k) record lists Thyssenkrupp Accessibility B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOW2, SWING?
The FDA product code for FLOW2, SWING is ILK.
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 Thyssenkrupp Accessibility B.V. 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: ILK)
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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