PNEU-WAVE— 510(k) K911574

Substantially Equivalent

Pneu-Mobility, Inc.

FDA 510(k) clearance K911574 for PNEU-WAVE, Substantially Equivalent on 1991-10-02. Applicant: Pneu-Mobility, Inc.. Device class: 2.

Clearance details

Applicant: Pneu-Mobility, Inc.
Product code: Code JFB
Device class: Class 2
Regulation: 21 CFR 890.5880
Advisory panel: Physical Medicine
Date received: 1991-04-08
Decision date: 1991-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethlehem, PA, 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.