BLOOD SAMPLING SET
K-Number: K103165 · 2010-11-10
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Device Summary
Frequently Asked Questions
What is the BLOOD SAMPLING SET?
BLOOD SAMPLING SET is a medical device that received FDA 510(k) clearance on 2010-11-10. The listed applicant is Acacia, Inc.. The 510(k) number is K103165.
When did BLOOD SAMPLING SET receive FDA 510(k) clearance?
BLOOD SAMPLING SET received FDA 510(k) clearance on 2010-11-10, under 510(k) number K103165.
Who is the listed applicant for BLOOD SAMPLING SET?
The FDA 510(k) record lists Acacia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD SAMPLING SET?
The FDA product code for BLOOD SAMPLING SET is FPA.
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 Acacia, 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: FPA)
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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