View
K-Number: K253639 · 2026-01-08
ApplicantGE Healthcare
Decision Date2026-01-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
View is a medical device manufactured by GE Healthcare. It received FDA 510(k) clearance on 2026-01-08 under approval number K253639. 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 View?
View is a medical device that received FDA 510(k) clearance on 2026-01-08. It is manufactured by GE Healthcare. The 510(k) number is K253639.
When was View approved by the FDA?
View received FDA 510(k) clearance on 2026-01-08, under approval number K253639.
What company makes View?
View is manufactured by GE Healthcare.
What is the FDA product code for View?
The FDA product code for View is LLZ.
Related Clinical Trials
NCT06702917
GSI Cardiac on Revolution Apex - US
RECRUITING
NCT07263815
EQUIP - Evaluation of Quality of Imaging on a Next-generation Total Body Pet Scan in Comparison to Conventional PET
ACTIVE_NOT_RECRUITING
NCT07496918
Brain Effects of Gamma Frequency Sensory Stimulation (40Hz Light, Sound and Other Devices)
RECRUITING
Other Devices by GE Healthcare
Related Devices (Code: LLZ)
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.