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

EAZY PRIMER

K Number: K142848 · Decision Feb 24, 2015
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
53
Review Days
147

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Basic Information

Device Name
EAZY PRIMER
K Number
K142848
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Parkell, Inc.
Date Received
September 30, 2014
Decision Date
February 24, 2015
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

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Other Clearances by Parkell, Inc.

K Number Device Name
K243254 Parkell Pit and Fissure Sealant
K210259 Parkell Self-Adhesive Cement
K191103 Parkell Desensitizer Gel
K190930 SmarTemp X1
K182296 HyperFil-LV
K172176 Parkell Universal Adhesive
K151518 BRUSH&BOND PLUS
K132115 ABSOLUTE DENTIN 2
K113839 RETRACT GINGIVAL RETRACTION/HEMOSTATIC PASTE
K101044 RETRIEVE IMPLANT CEMENT
Search all 53 clearances from Parkell, Inc. →