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

CONTACT SEAL

K Number: K802682 · Decision Nov 24, 1980
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
130
Applicant Total
17
Review Days
27

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Basic Information

Device Name
CONTACT SEAL
K Number
K802682
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3765
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Vivadent (Usa), Inc.
Date Received
October 28, 1980
Decision Date
November 24, 1980
Product Code
EBC
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
EBC Sealant, Pit And Fissure, And Conditioner

Similar 510(k) Clearances

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

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Other Clearances by Vivadent (Usa), Inc.

K Number Device Name
K863831 VIVADENT FILPIN
K823409 HELIOSIT-ORTHODONTIC
K813015 HELIOSEAL
K802679 SILANIT
K802681 HELIOBOND
K802683 HELIOSIT
K802684 HELIOMAT
K802685 REOLIT
K802680 ISOPAST-DS
K801227 SILICAP
Search all 17 clearances from Vivadent (Usa), Inc. →