FDA 510(k) FDA class 1 Substantially Equivalent 🇯🇵 Japan

NLZ Motor System

K Number: K163402 · Decision Aug 31, 2017
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
60
Applicant Total
40
Review Days
269

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NLZ Motor System
K Number
K163402
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nakanishi, Inc.
Date Received
December 5, 2016
Decision Date
August 31, 2017
Product Code
EBW
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
EBW Controller, Foot, Handpiece And Cord

Similar 510(k) Clearances

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

View all

Other Clearances by Nakanishi, Inc.

K Number Device Name
K260773 Varios Combi Pro2
K254163 VarioSurg 4
K251689 VARIOS 170 LUX SCALER SYSTEM (VA170LUXS10); VARIOS 170 LUX SCALER SYSTEM (VA170LUXS11); VARIOS 170 SCALER SYSTEM (VA170S11)
K252662 UniBur
K241880 Air Powered Tooth Polishing System (Perio-Mate); Air Powered Tooth Polishing System (Perio Mate Nozzle Tip)
K233288 NLZ Built-In Motor System
K233117 Surgic Pro2 (Surgic Pro2 OPT), Surgic Pro2 (Surgic Pro2 NON-OPT)
K233308 Air Motor (Model name: FX204 M4); Air Motor (Model name: M205)
K230888 Titanium Turbine
K230106 General Cutting Straight
Search all 40 clearances from Nakanishi, Inc. →