K802224Unknown

Quintrex 0516 Prog. Pulse Generator Sys

Name: K802224 Quintrex 0516 Prog. Pulse Generator Sys
Creator: Medcor, Inc.
Published: 1980-09-12
License: https://open.fda.gov/license/

Medcor, Inc., Mchenry IL / Traditional, Unknown

FDA source

K802224 is the FDA 510(k) clearance record for QUINTREX 0516 PROG. PULSE GENERATOR SYS, cleared for Medcor, Inc. on 1980-09-12. FDA records list 8 510(k) clearances for Medcor, Inc., from 1977-04-07 to 1980-11-19. As of 2026-09-10, FDA records show no recalls naming K802224.

Clearance record

Decision date: 1980-09-12
Received: 1980-09-12 (0 days to decision)
Review panel: Unknown
Applicant: Medcor, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No