Atlas FDA

RALCO

FDA 510(k) clearance K110856 · decided 2011-08-10

Clearance details

K-number
K110856
Device name
RALCO
Applicant
Ralco S.R.L.
Decision
Substantially Equivalent
Date received
2011-03-28
Decision date
2011-08-10
Days to decision
135 days
Clearance type
Traditional
Product code
IZX
Device class
2
Regulation number
892.1610
Medical specialty
Radiology
Advisory committee
Radiology
Location
Naples, FL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.