K850172Substantially Equivalent
Elekiban Magneto-Therapeutic Device
Mns, Ltd., Washington DC / Traditional, Substantially Equivalent
K850172 is the FDA 510(k) clearance record for ELEKIBAN MAGNETO-THERAPEUTIC DEVICE, cleared for Mns, Ltd. on . FDA records list one 510(k) clearance for Mns, Ltd. As of , FDA records show no recalls naming K850172.
Clearance record
- Decision date
- Received
- (90 days to decision)
- Review panel
- Unknown
- Applicant
- Mns, Ltd. 1575 Eye St. NW, Washington DC
- Third party review
- No
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