FDA 510(k) FDA class 1 Substantially Equivalent 🇫🇮 Finland

PROSTYLE COMPACT

K Number: K963209 · Decision Oct 24, 1996
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
28
Review Days
69

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Basic Information

Device Name
PROSTYLE COMPACT
K Number
K963209
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Planmeca Oy
Date Received
August 16, 1996
Decision Date
October 24, 1996
Product Code
KLC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
KLC Chair, Dental, With Operative Unit

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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 →