510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K844788Substantially Equivalent

Soleo Sunbed

Hapro International B.V., Memphis TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844788 is the FDA 510(k) clearance record for SOLEO SUNBED, cleared for Hapro International B.V. on . FDA records list one 510(k) clearance for Hapro International B.V. As of , FDA records show no recalls naming K844788.

Clearance record

Decision date
Received
(59 days to decision)
Review panel
Unknown
Applicant
Hapro International B.V. 5475 Crestview Dr., Memphis TN
Third party review
No