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

TAKE 1 ADVANCED RIGID TRAY

K Number: K092176 · Decision Jan 28, 2010
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
25
Review Days
191

Basic Information

Device Name
TAKE 1 ADVANCED RIGID TRAY
K Number
K092176
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KERR CORPORATION
Date Received
July 21, 2009
Decision Date
January 28, 2010
Product Code
ELW
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
ELW Material, Impression

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Other Clearances by KERR CORPORATION

K Number Device Name
K162948 Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated Retraction Cord/Materials
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K162536 GingiKnit+, GingiBraid+, GingiBraid+ Shortcut, and UniBraid+ impregnated Aluminum Potassium Sulfate Retraction Cord
K162164 GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord
K160441 Identic and KromaFaze Alginate Dental Impression Materials
K123468 DEMI ULTRA
K123595 NEXUS RMGI
K110747 TEMPFLEX
K110092 TAKE 1 ADVANCED RIGID TRAY
K102621 SOLSTICE
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