MEBIASIS AGAR GEL DIFFUSION KIT— 510(k) K854230

Name: FDA 510(k) clearance K854230
Creator: U.S. Food and Drug Administration
Published: 1985-11-12

Substantially Equivalent

Lmd Laboratories

FDA 510(k) clearance K854230 for MEBIASIS AGAR GEL DIFFUSION KIT, Substantially Equivalent on 1985-11-12. Applicant: Lmd Laboratories. Device class: 2.

Clearance details

Applicant: Lmd Laboratories
Product code: Code KHW
Device class: Class 2
Regulation: 21 CFR 866.3220
Advisory panel: Microbiology
Date received: 1985-10-21
Decision date: 1985-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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