K821852Substantially Equivalent

Diagnostics Hdl Cholesterol Precipitant

Name: K821852 Diagnostics Hdl Cholesterol Precipitant
Creator: Boehringer Mannheim Corp.
Published: 1982-07-02
License: https://open.fda.gov/license/

Boehringer Mannheim Corp., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K821852 is the FDA 510(k) clearance record for DIAGNOSTICS HDL CHOLESTEROL PRECIPITANT, cleared for Boehringer Mannheim Corp. on 1982-07-02. FDA records list 340 510(k) clearances for Boehringer Mannheim Corp., from 1976-10-08 to 1999-02-08. As of 2026-09-10, FDA records show no recalls naming K821852.

Clearance record

Decision date: 1982-07-02
Received: 1982-06-23 (9 days to decision)
Review panel: Unknown
Applicant: Boehringer Mannheim Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No