Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MOORFLPI FULL-FIELD LASER PERFUSION IMAGER

K-Number: K063586 · 2007-01-25

Decision Date2007-01-25
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOORFLPI 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 2007-01-25 under 510(k) number K063586. 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 FULL-FIELD LASER PERFUSION IMAGER?

MOORFLPI FULL-FIELD LASER PERFUSION IMAGER is a medical device that received FDA 510(k) clearance on 2007-01-25. The listed applicant is Moor Instruments, Ltd.. The 510(k) number is K063586.

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

MOORFLPI FULL-FIELD LASER PERFUSION IMAGER received FDA 510(k) clearance on 2007-01-25, under 510(k) number K063586.

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

The FDA product code for MOORFLPI 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

View on FDA Database →

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

↑