MRCAT Pelvis
K-Number: K182888 · 2019-04-30
ApplicantPhilips Medical Systems MR Finland
Decision Date2019-04-30
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MRCAT Pelvis is a medical device manufactured by Philips Medical Systems MR Finland. It received FDA 510(k) clearance on 2019-04-30 under approval number K182888. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MRCAT Pelvis?
MRCAT Pelvis is a medical device that received FDA 510(k) clearance on 2019-04-30. It is manufactured by Philips Medical Systems MR Finland. The 510(k) number is K182888.
When was MRCAT Pelvis approved by the FDA?
MRCAT Pelvis received FDA 510(k) clearance on 2019-04-30, under approval number K182888.
What company makes MRCAT Pelvis?
MRCAT Pelvis is manufactured by Philips Medical Systems MR Finland.
What is the FDA product code for MRCAT Pelvis?
The FDA product code for MRCAT Pelvis is MUJ.
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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.