CARDIOBEEPER CB250— 510(k) K983582

Substantially Equivalent

Merdian Medical Technologies , Ltd.

FDA 510(k) clearance K983582 for CARDIOBEEPER CB250, Substantially Equivalent on 1998-11-13. Applicant: Merdian Medical Technologies , Ltd..

Clearance details

Applicant: Merdian Medical Technologies , Ltd.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1998-10-13
Decision date: 1998-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Antrium, IE

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