Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K760214Substantially Equivalent

Stimulator, Pneumatic

O. F. Anderson, Mchenry IL / Traditional, Substantially Equivalent

K760214 is the FDA 510(k) clearance record for STIMULATOR, PNEUMATIC, cleared for O. F. Anderson on . FDA records list one 510(k) clearance for O. F. Anderson. As of , FDA records show no recalls naming K760214.

Clearance record

Decision date
Received
(193 days to decision)
Review panel
Unknown
Applicant
O. F. Anderson 803 N. Front St. Suite 3, Mchenry IL
Third party review
No