K870171Substantially Equivalent

(Merifluor)tm-Cryptosporidium

Name: K870171 (Merifluor)tm-Cryptosporidium
Creator: Meridian Diagnostics, Inc.
Published: 1987-03-16
License: https://open.fda.gov/license/

Meridian Diagnostics, Inc., Cincinnati OH / Traditional, Substantially Equivalent

FDA source

K870171 is the FDA 510(k) clearance record for (MERIFLUOR)TM-CRYPTOSPORIDIUM, cleared for Meridian Diagnostics, Inc. on 1987-03-16. FDA records list 92 510(k) clearances for Meridian Diagnostics, Inc., from 1980-01-17 to 1999-12-10. As of 2026-09-10, FDA records show no recalls naming K870171.

Clearance record

Decision date: 1987-03-16
Received: 1987-01-14 (61 days to decision)
Review panel: Unknown
Applicant: Meridian Diagnostics, Inc. 3471 River Hills Dr., Cincinnati OH
Third party review: No