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

J. MORITA AZ ULTRASONIC SYSTEM

K Number: K053030 · Decision Nov 7, 2005
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
194
Applicant Total
52
Review Days
11

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
J. MORITA AZ ULTRASONIC SYSTEM
K Number
K053030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
J. Morita USA, Inc.
Date Received
October 27, 2005
Decision Date
November 7, 2005
Product Code
ELC
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
ELC Scaler, Ultrasonic

Similar 510(k) Clearances

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

View all

Other Clearances by J. Morita USA, Inc.

K Number Device Name
K213477 Root ZX3
K201378 3D Accuitomo 150N
K190509 Lubrina 2
K173920 LS OIL
K171012 Veraview X800
K170275 Tri Auto ZX2
K120377 ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A
K112665 TRI AUTO MINI - ENDODEONTIC TREATMENT MOTORIZED HANDPIECE
K103697 TORQTECH
K090925 MULTIPLE (APEX LOCATOR), MODEL RCM-7
Search all 52 clearances from J. Morita USA, Inc. →