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

SEALITE

K Number: K862284 · Decision Jun 23, 1986
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
130
Applicant Total
37
Review Days
7

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Basic Information

Device Name
SEALITE
K Number
K862284
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3765
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Sybron Corp.
Date Received
June 16, 1986
Decision Date
June 23, 1986
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

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Other Clearances by Sybron Corp.

K Number Device Name
K854855 PROOF ALGINATE IMPRESSION MATERIAL
K844092 DIAGNOSTIC MICROSOPCE SLIDES
K842132 TYCOS SELF-CHECK/DIGITAL FEVER THERMO
K841910 KERR SEALAPEX ROOT CANAL SEALER
K841732 LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM
K840469 TYCOS SELF CHECK BPM3 BLOOD PRESS MONI
K840407 KERR RESIN BONDED BRIDGE CEMENT
K840607 LF MOTORIZED RADIOGRAPHIC FILM VIEWER
K833138 DIGITAL INJECTOR SYS
K823795 EVERBOND GLASS IONOMER CEMENT
Search all 37 clearances from Sybron Corp. →