SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION
K-Number: K101850 · 2011-03-02
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Device Summary
Frequently Asked Questions
What is the SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION?
SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION is a medical device that received FDA 510(k) clearance on 2011-03-02. The listed applicant is Spacelabs Healthcare, Ltd.. The 510(k) number is K101850.
When did SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION receive FDA 510(k) clearance?
SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION received FDA 510(k) clearance on 2011-03-02, under 510(k) number K101850.
Who is the listed applicant for SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION?
The FDA 510(k) record lists Spacelabs Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION?
The FDA product code for SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION is CBK.
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 Spacelabs Healthcare, Ltd. 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: CBK)
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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