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

FINESSE

K Number: K790585 · Decision May 16, 1979
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
20
Review Days
50

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Basic Information

Device Name
FINESSE
K Number
K790585
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
L.D. Caulk Co.
Date Received
March 27, 1979
Decision Date
May 16, 1979
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

Similar 510(k) Clearances

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

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Other Clearances by L.D. Caulk Co.

K Number Device Name
K802262 COMPOSITE RESTORATIVE
K801690 VALIANT
K790586 CHEMBOND
K780560 DENTAL AMALGAMATOR
K780384 IMPROVED DYCAL
K780301 CAULK TYLOK
K771398 SHELL VENEER
K771402 NUVA-COTE (MODIFICATION TO)
K771399 LIP & CHEEK RETRACTOR
K771400 IMPREGNATED DENTAL FLOSS
Search all 20 clearances from L.D. Caulk Co. →