PASTURE, MODELS: F550, A520— 510(k) K083176

Name: FDA 510(k) clearance K083176
Creator: U.S. Food and Drug Administration
Published: 2009-01-23

Substantially Equivalent

Pasture Pharma Pte, Ltd.

FDA 510(k) clearance K083176 for PASTURE, MODELS: F550, A520, Substantially Equivalent on 2009-01-23. Applicant: Pasture Pharma Pte, Ltd.. Device class: 2.

Clearance details

Applicant: Pasture Pharma Pte, Ltd.
Product code: Code NZJ
Device class: Class 2
Regulation: 21 CFR 880.6260
Advisory panel: General Hospital
Date received: 2008-10-28
Decision date: 2009-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Murrieta, CA, US

Download summary PDF View on FDA.gov ↗

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