K240040

VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)

510(k) number: K240040
Device name: VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)
Applicant: VATECH Co., Ltd. KR
Product code: MUH — System, X-Ray, Extraoral Source, Digital
Decision date: 2024-10-25
Date received: 2024-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: Dental

PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain

Also available from FDA: K240040.pdf

Official FDA record: K240040

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.