Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INGUINAL COMPRESSIVE DEVICE (ICD)

K-Number: K761092 · 1976-12-16

ApplicantMedical Electronic Devices, Inc.
Decision Date1976-12-16
Product Code
DecisionSubstantially Equivalent

Device Summary

INGUINAL COMPRESSIVE DEVICE (ICD) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Electronic Devices, Inc.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761092. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INGUINAL COMPRESSIVE DEVICE (ICD)?

INGUINAL COMPRESSIVE DEVICE (ICD) is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Medical Electronic Devices, Inc.. The 510(k) number is K761092.

When did INGUINAL COMPRESSIVE DEVICE (ICD) receive FDA 510(k) clearance?

INGUINAL COMPRESSIVE DEVICE (ICD) received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761092.

Who is the listed applicant for INGUINAL COMPRESSIVE DEVICE (ICD)?

The FDA 510(k) record lists Medical Electronic Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Electronic Devices, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K052563INOGEN SATELLITE CONSERVER, MODEL SC-100K033197INOGEN SATELLITE CONSERVERK023420PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEBK983601DEMAND OXYGEN CONSERVING DEVICE, DOCD, THE DOCK983459PULSED OXYGEN CONSERVING DEVICE, POCDK770115ARTERIAL DIAGNOSTIC UNIT (ADU)

View all 7 devices →

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑