Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K781157Substantially Equivalent

Stimulator, Nerve, Transcutaneous

Medtech Intl., Inc., Mchenry IL / Traditional, Substantially Equivalent

K781157 is the FDA 510(k) clearance record for STIMULATOR, NERVE, TRANSCUTANEOUS, cleared for Medtech Intl., Inc. on . FDA records list 6 510(k) clearances for Medtech Intl., Inc., from to . As of , FDA records show no recalls naming K781157.

Clearance record

Decision date
Received
(77 days to decision)
Review panel
Unknown
Applicant
Medtech Intl., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No