FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

eco-x Series (eco-x, eco-x-s)

K Number: K211159 · Decision Dec 30, 2021
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
9
Review Days
255

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
eco-x Series (eco-x, eco-x-s)
K Number
K211159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hdx Will Corp.
Date Received
April 19, 2021
Decision Date
December 30, 2021
Product Code
OAS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OAS X-Ray, Tomography, Computed, Dental

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OAS), ordered by most recent decision date.

View all

Other Clearances by Hdx Will Corp.

K Number Device Name
K211114 Will3D
K212254 DENTRIa series (DENTRIa, DENTRI-Ca, DENTRI-Sa)
K192700 Xcam
K190357 Star-X, Intraoral X-ray System
K181297 DENTIOIII series (DENTIOIII, DENTIOIII-S)
K172168 WillCeph
K170180 Will3D
K160140 DENTRIa series