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

COE-LITE POLYMERIZATION UNIT

K Number: K844325 · Decision Dec 11, 1984
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
20
Review Days
34

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Basic Information

Device Name
COE-LITE POLYMERIZATION UNIT
K Number
K844325
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Coe Laboratories, Inc.
Date Received
November 7, 1984
Decision Date
December 11, 1984
Product Code
EBZ
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
EBZ Activator, Ultraviolet, For Polymerization

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Other Clearances by Coe Laboratories, Inc.

K Number Device Name
K903292 ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS
K894282 FIRST IMPRESSION TM
K894281 FIRST IMPRESSION WITH CHLORHEXIDINE
K891140 OCCLU-SEAL(TM) VISIBLE LIGHT-CURED FISSURE SEALANT
K885010 TRIPTON(TM) VISIBLE LIGHT-CURED UNIV. BONDING
K881422 COE PAK AUTO MIX, REGULAR OR HARD SET
K881091 OMNISIL, VINYL POLYSILOXANE IMPRESSION MATERIAL
K863882 OPALUX VISIBLE LIGHT CURED ANTERIOR COMPOSITE
K842877 ABSOLUTE VINYL POLYSILOXANE IMPRESS
K844326 OCCLUSIN LIGHT CURED VISIBLE RADIOPAQUE COMPOSITE
Search all 20 clearances from Coe Laboratories, Inc. →