K800052Substantially Equivalent

Antimicrobial Removal Device (Ard)

Name: K800052 Antimicrobial Removal Device (Ard)
Creator: Marion Laboratories, Inc.
Published: 1980-04-04
License: https://open.fda.gov/license/

Marion Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K800052 is the FDA 510(k) clearance record for ANTIMICROBIAL REMOVAL DEVICE (ARD), cleared for Marion Laboratories, Inc. on 1980-04-04. FDA records list 38 510(k) clearances for Marion Laboratories, Inc., from 1978-03-22 to 1989-03-23. As of 2026-09-10, FDA records show no recalls naming K800052.

Clearance record

Decision date: 1980-04-04
Received: 1980-01-09 (86 days to decision)
Review panel: Unknown
Applicant: Marion Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No