ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE
K-Number: K912563 · 1991-10-02
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Device Summary
Frequently Asked Questions
What is the ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE?
ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is Mbo Laboratories, Inc.. The 510(k) number is K912563.
When did ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE receive FDA 510(k) clearance?
ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE received FDA 510(k) clearance on 1991-10-02, under 510(k) number K912563.
Who is the listed applicant for ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE?
The FDA 510(k) record lists Mbo Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE?
The FDA product code for ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE is FOZ.
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 Mbo Laboratories, 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: FOZ)
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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