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

COE PAK AUTO MIX, REGULAR OR HARD SET

K Number: K881422 · Decision Oct 31, 1988
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
20
Review Days
209

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Basic Information

Device Name
COE PAK AUTO MIX, REGULAR OR HARD SET
K Number
K881422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Coe Laboratories, Inc.
Date Received
April 5, 1988
Decision Date
October 31, 1988
Product Code
EMA
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
EMA Cement, Dental

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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
K881091 OMNISIL, VINYL POLYSILOXANE IMPRESSION MATERIAL
K863882 OPALUX VISIBLE LIGHT CURED ANTERIOR COMPOSITE
K842877 ABSOLUTE VINYL POLYSILOXANE IMPRESS
K844325 COE-LITE POLYMERIZATION UNIT
K844326 OCCLUSIN LIGHT CURED VISIBLE RADIOPAQUE COMPOSITE
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