DUAL GRAPH (TM) RECORDER-MONITOR— 510(k) K890711

Name: FDA 510(k) clearance K890711
Creator: U.S. Food and Drug Administration
Published: 1989-06-02

Substantially Equivalent

Somatics, Inc.

FDA 510(k) clearance K890711 for DUAL GRAPH (TM) RECORDER-MONITOR, Substantially Equivalent on 1989-06-02. Applicant: Somatics, Inc.. Device class: 1.

Clearance details

Applicant: Somatics, Inc.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1989-02-13
Decision date: 1989-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Bluff, IL, US

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