Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K830947Substantially Equivalent

Syringe/needle Dispos-Box-Cutter/crimper

Post Medical, Inc., Mchenry IL / Traditional, Substantially Equivalent

K830947 is the FDA 510(k) clearance record for SYRINGE/NEEDLE DISPOS-BOX-CUTTER/CRIMPER, cleared for Post Medical, Inc. on . FDA records list 6 510(k) clearances for Post Medical, Inc., from to . As of , FDA records show no recalls naming K830947.

Clearance record

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