BLOOD HAND PUMP ADMINISTRATION SET
K-Number: K050115 · 2005-04-01
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Device Summary
Frequently Asked Questions
What is the BLOOD HAND PUMP ADMINISTRATION SET?
BLOOD HAND PUMP ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 2005-04-01. The listed applicant is Cardinal Health, Alaris Products. The 510(k) number is K050115.
When did BLOOD HAND PUMP ADMINISTRATION SET receive FDA 510(k) clearance?
BLOOD HAND PUMP ADMINISTRATION SET received FDA 510(k) clearance on 2005-04-01, under 510(k) number K050115.
Who is the listed applicant for BLOOD HAND PUMP ADMINISTRATION SET?
The FDA 510(k) record lists Cardinal Health, Alaris Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD HAND PUMP ADMINISTRATION SET?
The FDA product code for BLOOD HAND PUMP ADMINISTRATION SET is BRZ.
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 Cardinal Health, Alaris Products 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: BRZ)
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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