ECHO-COM FOR MS-WINDOWS VERSION 2.0— 510(k) K960665

Substantially Equivalent

Cone Instruments, Inc.

FDA 510(k) clearance K960665 for ECHO-COM FOR MS-WINDOWS VERSION 2.0, Substantially Equivalent on 1996-05-07. Applicant: Cone Instruments, Inc..

Clearance details

Applicant: Cone Instruments, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1996-02-20
Decision date: 1996-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solon, OH, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.