PULSTAR LOGIX INTERMITTENT PNEUMATIC COMPRESSION SYSTEM— 510(k) K123308

Name: FDA 510(k) clearance K123308
Creator: U.S. Food and Drug Administration
Published: 2013-02-08

Substantially Equivalent

Albahealth, LLC

FDA 510(k) clearance K123308 for PULSTAR LOGIX INTERMITTENT PNEUMATIC COMPRESSION SYSTEM, Substantially Equivalent on 2013-02-08. Applicant: Albahealth, LLC. Device class: 2.

Clearance details

Applicant: Albahealth, LLC
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2012-10-24
Decision date: 2013-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockwood, TN, US

Download summary PDF View on FDA.gov ↗

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