K827501Substantially Equivalent

Model 580 Digital Radiography System

Name: K827501 Model 580 Digital Radiography System
Creator: Technicare Corp.
Published: 1982-06-09
License: https://open.fda.gov/license/

Technicare Corp., Solon OH / Traditional, Substantially Equivalent

FDA source

K827501 is the FDA 510(k) clearance record for MODEL 580 DIGITAL RADIOGRAPHY SYSTEM, cleared for Technicare Corp. on 1982-06-09. 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 K827501.

Clearance record

Decision date: 1982-06-09
Received: 1982-05-10 (30 days to decision)
Review panel: Unknown
Applicant: Technicare Corp. 29100 Aurora Rd., Solon OH
Third party review: No