K831666Substantially Equivalent

Sialography Needle

Name: K831666 Sialography Needle
Creator: Vertex Medical Corp.
Published: 1983-07-12
License: https://open.fda.gov/license/

Vertex Medical Corp., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K831666 is the FDA 510(k) clearance record for SIALOGRAPHY NEEDLE, cleared for Vertex Medical Corp. on 1983-07-12. FDA records list 21 510(k) clearances for Vertex Medical Corp., from 1982-09-21 to 1984-04-24. As of 2026-09-10, FDA records show no recalls naming K831666.

Clearance record

Decision date: 1983-07-12
Received: 1983-05-23 (50 days to decision)
Review panel: Unknown
Applicant: Vertex Medical Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No