CARDIOBEEPER CB-12L— 510(k) K965101

Substantially Equivalent

Meridian Medical Technologies, Inc.

FDA 510(k) clearance K965101 for CARDIOBEEPER CB-12L, Substantially Equivalent on 1997-03-17. Applicant: Meridian Medical Technologies, Inc..

Clearance details

Applicant: Meridian Medical Technologies, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1996-12-20
Decision date: 1997-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

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