MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR
K-Number: K032841 · 2003-12-10
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Device Summary
Frequently Asked Questions
What is the MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR?
MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR is a medical device that received FDA 510(k) clearance on 2003-12-10. The listed applicant is Moor Instruments, Ltd.. The 510(k) number is K032841.
When did MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR receive FDA 510(k) clearance?
MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR received FDA 510(k) clearance on 2003-12-10, under 510(k) number K032841.
Who is the listed applicant for MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR?
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 MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR?
The FDA product code for MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR 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.
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.
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