K761092Substantially Equivalent

Inguinal Compressive Device (Icd)

Name: K761092 Inguinal Compressive Device (Icd)
Creator: Medical Electronic Devices, Inc.
Published: 1976-12-16
License: https://open.fda.gov/license/

Medical Electronic Devices, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K761092 is the FDA 510(k) clearance record for INGUINAL COMPRESSIVE DEVICE (ICD), cleared for Medical Electronic Devices, Inc. on 1976-12-16. FDA records list 7 510(k) clearances for Medical Electronic Devices, Inc., from 1976-12-16 to 2005-10-24. As of 2026-09-10, FDA records show no recalls naming K761092.

Clearance record

Decision date: 1976-12-16
Received: 1976-11-22 (24 days to decision)
Review panel: Unknown
Applicant: Medical Electronic Devices, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No