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

VISTADENT OC - VERSION 4

K Number: K060836 · Decision Oct 27, 2006
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
12
Review Days
213

Basic Information

Device Name
VISTADENT OC - VERSION 4
K Number
K060836
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DENTSPLY INTL., INC.
Date Received
March 28, 2006
Decision Date
October 27, 2006
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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