K842406Substantially Equivalent

Wescott Type Biopsy Needle

Name: K842406 Wescott Type Biopsy Needle
Creator: Popper & Sons, Inc.
Published: 1984-08-09
License: https://open.fda.gov/license/

Popper & Sons, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K842406 is the FDA 510(k) clearance record for WESCOTT TYPE BIOPSY NEEDLE, cleared for Popper & Sons, Inc. on 1984-08-09. FDA records list 8 510(k) clearances for Popper & Sons, Inc., from 1984-03-12 to 1991-05-20. As of 2026-09-10, FDA records show no recalls naming K842406.

Clearance record

Decision date: 1984-08-09
Received: 1984-06-19 (51 days to decision)
Review panel: Unknown
Applicant: Popper & Sons, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No