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

FLUOR PROTECTOR

K Number: K946032 · Decision Mar 7, 1995
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
131
Review Days
88

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Basic Information

Device Name
FLUOR PROTECTOR
K Number
K946032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3260
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ivoclar North America, Inc.
Date Received
December 9, 1994
Decision Date
March 7, 1995
Product Code
LBH
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
LBH Varnish, Cavity

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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. →