ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000— 510(k) K984405

Name: FDA 510(k) clearance K984405
Creator: U.S. Food and Drug Administration
Published: 1999-02-08

Substantially Equivalent

Intracom Corp.

FDA 510(k) clearance K984405 for ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000, Substantially Equivalent on 1999-02-08. Applicant: Intracom Corp.. Device class: 1.

Clearance details

Applicant: Intracom Corp.
Product code: Code LMB
Device class: Class 1
Regulation: 21 CFR 892.2010
Advisory panel: Radiology
Date received: 1998-12-09
Decision date: 1999-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

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