XLD AGAR (XYLASE LYSINE DESOXY AGAR)— 510(k) K791477

Name: FDA 510(k) clearance K791477
Creator: U.S. Food and Drug Administration
Published: 1979-09-04

Substantially Equivalent

Isle Media and Sterile Products, Inc.

FDA 510(k) clearance K791477 for XLD AGAR (XYLASE LYSINE DESOXY AGAR), Substantially Equivalent on 1979-09-04. Applicant: Isle Media and Sterile Products, Inc.. Device class: 1.

Clearance details

Applicant: Isle Media and Sterile Products, Inc.
Product code: Code JSI
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1979-07-30
Decision date: 1979-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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