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FDA 510(k)

DEMASQ IMAGING SPFTWARE DEVICE

K-Number: K090481 · 2009-03-19

ApplicantDemasq Limited
Decision Date2009-03-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DEMASQ IMAGING SPFTWARE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Demasq Limited. It received FDA 510(k) clearance on 2009-03-19 under 510(k) number K090481. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEMASQ IMAGING SPFTWARE DEVICE?

DEMASQ IMAGING SPFTWARE DEVICE is a medical device that received FDA 510(k) clearance on 2009-03-19. The listed applicant is Demasq Limited. The 510(k) number is K090481.

When did DEMASQ IMAGING SPFTWARE DEVICE receive FDA 510(k) clearance?

DEMASQ IMAGING SPFTWARE DEVICE received FDA 510(k) clearance on 2009-03-19, under 510(k) number K090481.

Who is the listed applicant for DEMASQ IMAGING SPFTWARE DEVICE?

The FDA 510(k) record lists Demasq Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEMASQ IMAGING SPFTWARE DEVICE?

The FDA product code for DEMASQ IMAGING SPFTWARE DEVICE is LLZ.

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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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