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

SYNTAC (DENTIN BONDING AGENT)

K Number: K901913 · Decision Jun 26, 1990
Classifications
1
FEI Numbers
133
Registration Numbers
133
Same Product Code
410
Applicant Total
131
Review Days
61

Basic Information

Device Name
SYNTAC (DENTIN BONDING AGENT)
K Number
K901913
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
IVOCLAR NORTH AMERICA, INC.
Date Received
April 26, 1990
Decision Date
June 26, 1990
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

Similar 510(k) Clearances

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Other Clearances by IVOCLAR NORTH AMERICA, INC.

K Number Device Name
K012174 ERIS LAYERING MATERIALS
K011491 HELIOSEAL CLEAR CHROMA
K011492 IN TEN-S
K011490 MODIFICATION TO EXCITE
K011023 D.SIGN 96
K011022 BIOUNIVERSAL PDF
K010381 D.SIGN 30
K010250 TETRIC CERAM HB
K003293 EXCITE DSC
K003407 SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)
Search all 131 clearances from IVOCLAR NORTH AMERICA, INC. →