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

ASC-12 PIEZOELECTRIC SCALER

K Number: K070866 · Decision Apr 11, 2007
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
194
Applicant Total
18
Review Days
13

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
ASC-12 PIEZOELECTRIC SCALER
K Number
K070866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aseptico, Inc.
Date Received
March 29, 2007
Decision Date
April 11, 2007
Product Code
ELC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

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 Aseptico, Inc.

K Number Device Name
K150129 AEU-7000L-70V IMPLANT/ENDODONTIC DENTAL SYSTEM (LIGHTED VERSION)
K142124 AEU-6000 IMPLANT / ENDODONTIC DENTAL SYSTEM
K130693 AEU-525 TRANSPORT III PORTABLE DENTAL SYSTEM
K111078 AEU-26L ELCTRONIC ENDODONTIC SYSTEM
K101332 AMC-20 PORTABLE DENTAL CART MODEL AMC-20
K103399 GENERAL DENISTRY MOTOR
K051077 E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101
K050201 AEU-14CF EXPENDITION
K030895 ASEPTICO ENDOPEX V, MODEL AEU-40
K030163 ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925
Search all 18 clearances from Aseptico, Inc. →