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

RAYPEX 6

K Number: K131907 · Decision Jan 31, 2014
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
36
Review Days
219

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Basic Information

Device Name
RAYPEX 6
K Number
K131907
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply International, Inc.
Date Received
June 26, 2013
Decision Date
January 31, 2014
Product Code
LQY
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
LQY Locator, Root Apex

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