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FDA 510(k)

MOOR LASER BLOOD FLOW MONITOR MBF3D

K-Number: K905233 · 1991-01-11

Decision Date1991-01-11
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MOOR LASER BLOOD FLOW MONITOR MBF3D is the device name listed in this FDA 510(k) record. The listed applicant is Moor Instruments, Ltd.. It received FDA 510(k) clearance on 1991-01-11 under 510(k) number K905233. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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