DCI MODEL EP-2 CLINICAL STIMULATOR— 510(k) K854196

Name: FDA 510(k) clearance K854196
Creator: U.S. Food and Drug Administration
Published: 1986-05-01

Substantially Equivalent

Digital Cardiovascular Instruments, Inc.

FDA 510(k) clearance K854196 for DCI MODEL EP-2 CLINICAL STIMULATOR, Substantially Equivalent on 1986-05-01. Applicant: Digital Cardiovascular Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Digital Cardiovascular Instruments, Inc.
Product code: Code DRO
Device class: Class 2
Regulation: 21 CFR 870.5550
Advisory panel: Cardiovascular
Date received: 1985-10-15
Decision date: 1986-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Emeryville, CA, US

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