K831520Substantially Equivalent

Morwel Cannula

Name: K831520 Morwel Cannula
Creator: Morwel Corp.
Published: 1983-06-20
License: https://open.fda.gov/license/

Morwel Corp., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K831520 is the FDA 510(k) clearance record for MORWEL CANNULA, cleared for Morwel Corp. on 1983-06-20. FDA records list 4 510(k) clearances for Morwel Corp., from 1983-06-20 to 1996-09-19. As of 2026-09-10, FDA records show no recalls naming K831520.

Clearance record

Decision date: 1983-06-20
Received: 1983-05-12 (39 days to decision)
Review panel: Unknown
Applicant: Morwel Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No