Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K800835Substantially Equivalent

Kandi-Nuclear Med. Data Acqu.&info.

Krupp International, Inc., Mchenry IL / Traditional, Substantially Equivalent

K800835 is the FDA 510(k) clearance record for KANDI-NUCLEAR MED. DATA ACQU.&INFO., cleared for Krupp International, Inc. on . FDA records list 2 510(k) clearances for Krupp International, Inc., from to . As of , FDA records show no recalls naming K800835.

Clearance record

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