ACTIVATOR II— 510(k) K973506

Name: FDA 510(k) clearance K973506
Creator: U.S. Food and Drug Administration
Published: 1998-01-27

Substantially Equivalent

Activator Methods, Inc.

FDA 510(k) clearance K973506 for ACTIVATOR II, Substantially Equivalent on 1998-01-27. Applicant: Activator Methods, Inc.. Device class: Unclassified.

Clearance details

Applicant: Activator Methods, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1997-09-16
Decision date: 1998-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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