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

COMMAND BONDING RESIN/GLAZE/OPAQUER

K Number: K822869 · Decision Oct 13, 1982
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
51
Applicant Total
37
Review Days
16

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Basic Information

Device Name
COMMAND BONDING RESIN/GLAZE/OPAQUER
K Number
K822869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3310
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Sybron Corp.
Date Received
September 27, 1982
Decision Date
October 13, 1982
Product Code
EBD
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
EBD Coating, Filling Material, Resin

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Other Clearances by Sybron Corp.

K Number Device Name
K862284 SEALITE
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
Search all 37 clearances from Sybron Corp. →