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

AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL

K Number: K863630 · Decision Mar 11, 1987
Classifications
1
FEI Numbers
167
Registration Numbers
167
Same Product Code
322
Applicant Total
19
Review Days
175

Basic Information

Device Name
AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL
K Number
K863630
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
AUSTENAL DENTAL, INC.
Date Received
September 17, 1986
Decision Date
March 11, 1987
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

Similar 510(k) Clearances

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

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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
K865025 AUSTENAL CONDENSING INSTRUMENT
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. →