Class Class II

Reprieve by RegenesisTM (K223620)

K223620 2023-05-24 Traditional
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Description

Reprieve by RegenesisTM by Regenesis Biomedical, Inc. — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223620
Clearance Date2023-05-24
Clearance TypeTraditional
Product CodeIMJ
Regulation Number890.5290

Categories

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