TRI-PLEX ADAPTER— 510(k) K010401

Substantially Equivalent

The Medical Device Group, Inc.

FDA 510(k) clearance K010401 for TRI-PLEX ADAPTER, Substantially Equivalent on 2002-10-30. Applicant: The Medical Device Group, Inc..

Clearance details

Applicant: The Medical Device Group, Inc.
Product code: Code MOD
Advisory panel: Anesthesiology
Date received: 2001-02-12
Decision date: 2002-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

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