NM/CT 850, NM/CT 860
K-Number: K173816 · 2018-04-17
ApplicantGE Healthcare
Decision Date2018-04-17
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
NM/CT 850, NM/CT 860 is a medical device manufactured by GE Healthcare. It received FDA 510(k) clearance on 2018-04-17 under approval number K173816. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NM/CT 850, NM/CT 860?
NM/CT 850, NM/CT 860 is a medical device that received FDA 510(k) clearance on 2018-04-17. It is manufactured by GE Healthcare. The 510(k) number is K173816.
When was NM/CT 850, NM/CT 860 approved by the FDA?
NM/CT 850, NM/CT 860 received FDA 510(k) clearance on 2018-04-17, under approval number K173816.
What company makes NM/CT 850, NM/CT 860?
NM/CT 850, NM/CT 860 is manufactured by GE Healthcare.
What is the FDA product code for NM/CT 850, NM/CT 860?
The FDA product code for NM/CT 850, NM/CT 860 is KPS.
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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.