FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AUSTENAL CONDENSING INSTRUMENT

K Number: K865025 · Decision Feb 19, 1987
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
2
Applicant Total
19
Review Days
58

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
AUSTENAL CONDENSING INSTRUMENT
K Number
K865025
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Austenal Dental, Inc.
Date Received
December 23, 1986
Decision Date
February 19, 1987
Product Code
EKG
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
EKG Condenser, Amalgam And Foil, Operative

Similar 510(k) Clearances

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

View all

Other Clearances by Austenal Dental, Inc.

K Number Device Name
K890713 OVERDENTURE - STUD ATTACHMENT
K883799 BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN
K880875 VITALLIUM EQUIPOISE ALLOY
K871849 LIGHT CURE DENTURE GLAZE
K872746 VITALLIUM WIRE
K863630 AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL
K862557 AUSTENAL ACUSOFT SOFT LINER
K864826 A-SP ALLOY (SILVER-PALLADIUM CROWN & BRIDGE ALLOY)
K862856 PALLADIUM BASED DENT ALLOYS/PORCELAIN METAL RESTOR
K862667 COBALT, 29.5% CHROMIUM ALLOY DENTAL BAKE-ON ALLOY
Search all 19 clearances from Austenal Dental, Inc. →