IMPULSE HVG— 510(k) K970847

Substantially Equivalent

Armstrong Industries, Inc.

FDA 510(k) clearance K970847 for IMPULSE HVG, Substantially Equivalent on 1997-09-10. Applicant: Armstrong Industries, Inc.. Device class: 2.

Clearance details

Applicant: Armstrong Industries, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1997-03-07
Decision date: 1997-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plano, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.