BRIDGE III RECEIVER— 510(k) K010794

Name: FDA 510(k) clearance K010794
Creator: U.S. Food and Drug Administration
Published: 2001-05-10

Substantially Equivalent

Meridian Medical Technologies , Ltd.

FDA 510(k) clearance K010794 for BRIDGE III RECEIVER, Substantially Equivalent on 2001-05-10. 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: 2001-03-16
Decision date: 2001-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Belfast, IE

Download summary PDF View on FDA.gov ↗

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