MODEL EP-2 CLINICAL STIMULATOR— 510(k) K933069

Name: FDA 510(k) clearance K933069
Creator: U.S. Food and Drug Administration
Published: 1993-10-21

Substantially Equivalent

Ep Medical, Inc.

FDA 510(k) clearance K933069 for MODEL EP-2 CLINICAL STIMULATOR, Substantially Equivalent on 1993-10-21. Applicant: Ep Medical, Inc.. Device class: 2.

Clearance details

Applicant: Ep Medical, Inc.
Product code: Code DTA
Device class: Class 2
Regulation: 21 CFR 870.3720
Advisory panel: Cardiovascular
Date received: 1993-06-22
Decision date: 1993-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Budd Lake, NJ, US

Download summary PDF View on FDA.gov ↗

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