K827610Substantially Equivalent

Ultrasound Auto Sector Cardiac Module

Name: K827610 Ultrasound Auto Sector Cardiac Module
Creator: Technicare Corp.
Published: 1982-07-20
License: https://open.fda.gov/license/

Technicare Corp., Solon OH / Traditional, Substantially Equivalent

FDA source

K827610 is the FDA 510(k) clearance record for ULTRASOUND AUTO SECTOR CARDIAC MODULE, cleared for Technicare Corp. on 1982-07-20. FDA records list 32 510(k) clearances for Technicare Corp., from 1980-05-14 to 1985-11-15. As of 2026-09-10, FDA records show no recalls naming K827610.

Clearance record

Decision date: 1982-07-20
Received: 1982-06-15 (35 days to decision)
Review panel: Unknown
Applicant: Technicare Corp. 29100 Aurora Rd., Solon OH
Third party review: No