Class Class II

MyoStrain (6.0) (K241607)

K241607 2024-08-26 Special
Home/ Devices/ MyoStrain (6.0) (K241607)

Description

MyoStrain (6.0) by Myocardial Solutions, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241607
Clearance Date2024-08-26
Clearance TypeSpecial
Product CodeLNH
Regulation Number892.1000

Categories

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