INTEGRATOR— 510(k) K950646

Name: FDA 510(k) clearance K950646
Creator: U.S. Food and Drug Administration
Published: 1996-04-30

Substantially Equivalent

Moyco Union Broach, Div., Moyco Technologies, Inc.

FDA 510(k) clearance K950646 for INTEGRATOR, Substantially Equivalent on 1996-04-30. Applicant: Moyco Union Broach, Div., Moyco Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Moyco Union Broach, Div., Moyco Technologies, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-02-13
Decision date: 1996-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: York, PA, US

Download summary PDF View on FDA.gov ↗

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