NM/CT 850, NM/CT 860
K-Number: K173816 · 2018-04-17
Device Summary
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. The listed applicant is GE Healthcare. The 510(k) number is K173816.
When did NM/CT 850, NM/CT 860 receive FDA 510(k) clearance?
NM/CT 850, NM/CT 860 received FDA 510(k) clearance on 2018-04-17, under 510(k) number K173816.
Who is the listed applicant for NM/CT 850, NM/CT 860?
The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.
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.
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 GE Healthcare 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: KPS)
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.