MOOORLDI LASER DOPPLER IMAGER
K-Number: K980383 · 1998-04-30
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Device Summary
Frequently Asked Questions
What is the MOOORLDI LASER DOPPLER IMAGER?
MOOORLDI LASER DOPPLER IMAGER is a medical device that received FDA 510(k) clearance on 1998-04-30. The listed applicant is Moor Instruments, Ltd.. The 510(k) number is K980383.
When did MOOORLDI LASER DOPPLER IMAGER receive FDA 510(k) clearance?
MOOORLDI LASER DOPPLER IMAGER received FDA 510(k) clearance on 1998-04-30, under 510(k) number K980383.
Who is the listed applicant for MOOORLDI LASER DOPPLER 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 MOOORLDI LASER DOPPLER IMAGER?
The FDA product code for MOOORLDI LASER DOPPLER 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.
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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