ADMIRE
K-Number: K153360 · 2016-06-29
ApplicantSiemens Medi Cal Solutions, Inc.
Decision Date2016-06-29
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ADMIRE is a medical device manufactured by Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2016-06-29 under approval number K153360. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ADMIRE?
ADMIRE is a medical device that received FDA 510(k) clearance on 2016-06-29. It is manufactured by Siemens Medi Cal Solutions, Inc.. The 510(k) number is K153360.
When was ADMIRE approved by the FDA?
ADMIRE received FDA 510(k) clearance on 2016-06-29, under approval number K153360.
What company makes ADMIRE?
ADMIRE is manufactured by Siemens Medi Cal Solutions, Inc..
What is the FDA product code for ADMIRE?
The FDA product code for ADMIRE is JAK.
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K171766Acuson SC2000 Diagnostic Ultrasound System
K170315Acuson SC2000 Diagnostic Ultrasound System
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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.