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

DENTIOIII series (DENTIOIII, DENTIOIII-S)

K Number: K181297 · Decision Nov 21, 2018
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
9
Review Days
189

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
DENTIOIII series (DENTIOIII, DENTIOIII-S)
K Number
K181297
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hdx Will Corp.
Date Received
May 16, 2018
Decision Date
November 21, 2018
Product Code
MUH
Advisory Committee
Dental
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
MUH System, X-Ray, Extraoral Source, Digital

Similar 510(k) Clearances

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

View all

Other Clearances by Hdx Will Corp.

K Number Device Name
K211159 eco-x Series (eco-x, eco-x-s)
K211114 Will3D
K212254 DENTRIa series (DENTRIa, DENTRI-Ca, DENTRI-Sa)
K192700 Xcam
K190357 Star-X, Intraoral X-ray System
K172168 WillCeph
K170180 Will3D
K160140 DENTRIa series