K852180Substantially Equivalent for Some Indications

Surgidynes Varidyne 350-2I & 350-2C Cordless Elec.

Name: K852180 Surgidynes Varidyne 350-2I & 350-2C Cordless Elec.
Creator: Surgidyne, Inc.
Published: 1985-07-01
License: https://open.fda.gov/license/

Surgidyne, Inc., Minneapolis MN / Traditional, Substantially Equivalent for Some Indications

FDA source

K852180 is the FDA 510(k) clearance record for SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC., cleared for Surgidyne, Inc. on 1985-07-01. FDA records list 6 510(k) clearances for Surgidyne, Inc., from 1985-06-28 to 1989-05-31. As of 2026-09-10, FDA records show no recalls naming K852180.

Clearance record

Decision date: 1985-07-01
Received: 1985-05-20 (42 days to decision)
Review panel: Unknown
Applicant: Surgidyne, Inc. 6975 Washington Ave., Minneapolis MN
Third party review: No