Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K772228Substantially Equivalent

Alsite Magnivision

Al Nyman & Son, Inc., Mchenry IL / Traditional, Substantially Equivalent

K772228 is the FDA 510(k) clearance record for ALSITE MAGNIVISION, cleared for Al Nyman & Son, Inc. on . FDA records list one 510(k) clearance for Al Nyman & Son, Inc. As of , FDA records show no recalls naming K772228.

Clearance record

Decision date
Received
(28 days to decision)
Review panel
Unknown
Applicant
Al Nyman & Son, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No