FDA 510(k) FDA unclassified Substantially Equivalent 🇮🇹 Italy

Apex Locator

K Number: K231990 · Decision Feb 13, 2024
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
21
Review Days
223

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Basic Information

Device Name
Apex Locator
K Number
K231990
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cefla S.C.
Date Received
July 5, 2023
Decision Date
February 13, 2024
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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K223794 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
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K220664 NewTom 7G
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