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

LifeRay Intraoral Handheld X-ray System

K Number: K241305 · Decision Jul 5, 2024
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
2
Review Days
57

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Basic Information

Device Name
LifeRay Intraoral Handheld X-ray System
K Number
K241305
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lucas Lifecare
Date Received
May 9, 2024
Decision Date
July 5, 2024
Product Code
EHD
Advisory Committee
Dental
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EHD Unit, X-Ray, Extraoral With Timer

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