RBM
K-Number: K020480 · 2002-03-12
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Device Summary
Frequently Asked Questions
What is the RBM?
RBM is a medical device that received FDA 510(k) clearance on 2002-03-12. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K020480.
When did RBM receive FDA 510(k) clearance?
RBM received FDA 510(k) clearance on 2002-03-12, under 510(k) number K020480.
Who is the listed applicant for RBM?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RBM?
The FDA product code for RBM is KGS.
Other records listing Smith & Nephew, 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: KGS)
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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