K827708Substantially Equivalent

Ultrasonic Medical Device Model 3 Lo 4

Name: K827708 Ultrasonic Medical Device Model 3 Lo 4
Creator: Sterisson
Published: 1983-04-12
License: https://open.fda.gov/license/

Sterisson, Mchenry IL / Traditional, Substantially Equivalent

FDA source

K827708 is the FDA 510(k) clearance record for ULTRASONIC MEDICAL DEVICE MODEL 3 LO 4, cleared for Sterisson on 1983-04-12. FDA records list one 510(k) clearance for Sterisson. As of 2026-09-10, FDA records show no recalls naming K827708.

Clearance record

Decision date: 1983-04-12
Received: 1982-07-12 (274 days to decision)
Review panel: Unknown
Applicant: Sterisson 803 N. Front St. Suite 3, Mchenry IL
Third party review: No