FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

TSC

K Number: K101756 · Decision Oct 26, 2010
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
35
Applicant Total
32
Review Days
125

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Basic Information

Device Name
TSC
K Number
K101756
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerr Corporation
Date Received
June 23, 2010
Decision Date
October 26, 2010
Product Code
MVL
Advisory Committee
Unknown
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
MVL Cord, Retraction

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K182162 OptiBond eXTRa Universal
K162948 Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated Retraction Cord/Materials
K163064 Demi Ultra
K162536 GingiKnit+, GingiBraid+, GingiBraid+ Shortcut, and UniBraid+ impregnated Aluminum Potassium Sulfate Retraction Cord
K162164 GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord
K162436 EndoVac Pure
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