ENHANCE HUMAN SERUM ALBUMIN— 510(k) K030850

Name: FDA 510(k) clearance K030850
Creator: U.S. Food and Drug Administration
Published: 2003-04-08

Substantially Equivalent

Conception Technologies

FDA 510(k) clearance K030850 for ENHANCE HUMAN SERUM ALBUMIN, Substantially Equivalent on 2003-04-08. Applicant: Conception Technologies. Device class: 2.

Clearance details

Applicant: Conception Technologies
Product code: Code MQL
Device class: Class 2
Regulation: 21 CFR 884.6180
Advisory panel: Obstetrics/Gynecology
Date received: 2003-03-17
Decision date: 2003-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, 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.