Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K020327
Device Classification Name
Controller, Foot, Handpiece And Cord
More FDA Info for this Device
510(K) Number
K020327
Device Name
Controller, Foot, Handpiece And Cord
Applicant
NAKANISHI, INC.
700 SHIMOHINATA
KANUMA-SHI, TOCHIGI-KEN 322-8666 JP
Other 510(k) Applications for this Company
Contact
HIROJI SEKIGUCHI
Other 510(k) Applications for this Contact
Regulation Number
872.4200
More FDA Info for this Regulation Number
Classification Product Code
EBW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/31/2002
Decision Date
04/08/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact