Class Class II

LM-9300 Plus Lithotripter (K213772)

K213772 2023-01-19 Traditional
Home/ Devices/ LM-9300 Plus Lithotripter (K213772)

Description

LM-9300 Plus Lithotripter by Lite-Med, Inc. — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213772
Clearance Date2023-01-19
Clearance TypeTraditional
Product CodeLNS
Regulation Number876.5990

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