FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT

K Number: K011619 · Decision Jun 29, 2001
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
28
Review Days
35

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Basic Information

Device Name
PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT
K Number
K011619
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, 2001
Decision Date
June 29, 2001
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

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Other Clearances by Planmeca Oy

K Number Device Name
K230985 Planmeca Viso
K200572 Planmeca Romexis
K181576 Planmeca Viso
K171385 Planmeca Romexis
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
Search all 28 clearances from Planmeca Oy →