MOOR LASER BLOOD FLOW MONITOR MBF3D
K-Number: K905233 · 1991-01-11
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Device Summary
Frequently Asked Questions
What is the MOOR LASER BLOOD FLOW MONITOR MBF3D?
MOOR LASER BLOOD FLOW MONITOR MBF3D is a medical device that received FDA 510(k) clearance on 1991-01-11. The listed applicant is Moor Instruments, Ltd.. The 510(k) number is K905233.
When did MOOR LASER BLOOD FLOW MONITOR MBF3D receive FDA 510(k) clearance?
MOOR LASER BLOOD FLOW MONITOR MBF3D received FDA 510(k) clearance on 1991-01-11, under 510(k) number K905233.
Who is the listed applicant for MOOR LASER BLOOD FLOW MONITOR MBF3D?
The FDA 510(k) record lists Moor Instruments, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOOR LASER BLOOD FLOW MONITOR MBF3D?
The FDA product code for MOOR LASER BLOOD FLOW MONITOR MBF3D is GEX. This falls under the Gastroenterology category.
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 Moor Instruments, 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: GEX)
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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