INTERMITTENT COMPRESSION BOOT FOR OTC— 510(k) K991921

Name: FDA 510(k) clearance K991921
Creator: U.S. Food and Drug Administration
Published: 1999-08-13

Substantially Equivalent

Eischoco, Inc.

FDA 510(k) clearance K991921 for INTERMITTENT COMPRESSION BOOT FOR OTC, Substantially Equivalent on 1999-08-13. Applicant: Eischoco, Inc.. Device class: 2.

Clearance details

Applicant: Eischoco, Inc.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 1999-06-07
Decision date: 1999-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gresham, OR, US

Download summary PDF View on FDA.gov ↗

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