FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

PANORAMIC X-RAY UNIT (MODIFICATION)

K Number: K952763 · Decision Oct 7, 1995
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
183
Applicant Total
24
Review Days
135

Basic Information

Device Name
PANORAMIC X-RAY UNIT (MODIFICATION)
K Number
K952763
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
PLANMECA OY
Date Received
May 25, 1995
Decision Date
October 7, 1995
Product Code
EHD
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
EHD Unit, X-Ray, Extraoral With Timer

Similar 510(k) Clearances

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

View all

Other Clearances by PLANMECA OY

K Number Device Name
K160506 Planmeca ProMax 3D Max, Planmeca Maximity
K140713 PLANMECA ROMEXIS
K103689 PLANMECA PROMAX 3D MID
K093590 PLANMECA PROMAX 3D MAX
K091197 PLANMECA PROSENSOR
K072244 PLANMECA PROONE
K060328 PLANMECA PROMAX 3D
K051464 PLANMECA PROMAX WITH DEC (DYNAMIC EXPOSURE CONTROL)
K011619 PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT
K000771 DIMAX 2
Search all 24 clearances from PLANMECA OY →