K760223Substantially Equivalent

Scanner, Ultrasound Body/heart

Name: K760223 Scanner, Ultrasound Body/heart
Creator: Mediscra, Inc.
Published: 1976-09-07
License: https://open.fda.gov/license/

Mediscra, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K760223 is the FDA 510(k) clearance record for SCANNER, ULTRASOUND BODY/HEART, cleared for Mediscra, Inc. on 1976-09-07. FDA records list one 510(k) clearance for Mediscra, Inc. As of 2026-09-10, FDA records show no recalls naming K760223.

Clearance record

Decision date: 1976-09-07
Received: 1976-07-12 (57 days to decision)
Review panel: Unknown
Applicant: Mediscra, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No