SWANNSHIDI BONE MARROW ASPIRATION NEEDLE
K-Number: K121181 · 2012-08-22
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Device Summary
Frequently Asked Questions
What is the SWANNSHIDI BONE MARROW ASPIRATION NEEDLE?
SWANNSHIDI BONE MARROW ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 2012-08-22. The listed applicant is Alliance Partners, LLC. The 510(k) number is K121181.
When did SWANNSHIDI BONE MARROW ASPIRATION NEEDLE receive FDA 510(k) clearance?
SWANNSHIDI BONE MARROW ASPIRATION NEEDLE received FDA 510(k) clearance on 2012-08-22, under 510(k) number K121181.
Who is the listed applicant for SWANNSHIDI BONE MARROW ASPIRATION NEEDLE?
The FDA 510(k) record lists Alliance Partners, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SWANNSHIDI BONE MARROW ASPIRATION NEEDLE?
The FDA product code for SWANNSHIDI BONE MARROW ASPIRATION NEEDLE is KNW.
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 Alliance Partners, LLC 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: KNW)
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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