CARDIOBEEPER CB12/12, MODEL CB12/12— 510(k) K002310

Name: FDA 510(k) clearance K002310
Creator: U.S. Food and Drug Administration
Published: 2000-10-25

Substantially Equivalent

Meridian Medical Technologies , Ltd.

FDA 510(k) clearance K002310 for CARDIOBEEPER CB12/12, MODEL CB12/12, Substantially Equivalent on 2000-10-25. Applicant: Meridian Medical Technologies , Ltd.. Device class: 2.

Clearance details

Applicant: Meridian Medical Technologies , Ltd.
Product code: Code DXH
Device class: Class 2
Regulation: 21 CFR 870.2920
Advisory panel: Cardiovascular
Date received: 2000-07-31
Decision date: 2000-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Belfast, IE

Download summary PDF View on FDA.gov ↗

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