SAS LEGIONELLA TEST, SAS LEGIONELLA DIPSTICK TEST— 510(k) K061496

Name: FDA 510(k) clearance K061496
Creator: U.S. Food and Drug Administration
Published: 2007-06-28

Substantially Equivalent

Sa Scientific , Ltd.

FDA 510(k) clearance K061496 for SAS LEGIONELLA TEST, SAS LEGIONELLA DIPSTICK TEST, Substantially Equivalent on 2007-06-28. Applicant: Sa Scientific , Ltd.. Device class: 2.

Clearance details

Applicant: Sa Scientific , Ltd.
Product code: Code MJH
Device class: Class 2
Regulation: 21 CFR 866.3300
Advisory panel: Microbiology
Date received: 2006-05-31
Decision date: 2007-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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