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FDA 510(k)

MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER

K-Number: K122943 · 2013-01-03

Decision Date2013-01-03
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER 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 2013-01-03 under 510(k) number K122943. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER?

MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER is a medical device that received FDA 510(k) clearance on 2013-01-03. The listed applicant is Moor Instruments, Ltd.. The 510(k) number is K122943.

When did MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER receive FDA 510(k) clearance?

MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER received FDA 510(k) clearance on 2013-01-03, under 510(k) number K122943.

Who is the listed applicant for MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER?

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 MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER?

The FDA product code for MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER is DPT.

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.

View all 13 devices →

Related Devices (Code: DPT)

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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