LAKED BLOOD AGAR W/PAROMOMYCIN & VANCOM— 510(k) K823122

Name: FDA 510(k) clearance K823122
Creator: U.S. Food and Drug Administration
Published: 1982-12-03

Substantially Equivalent

Granite Diagnostics, Inc.

FDA 510(k) clearance K823122 for LAKED BLOOD AGAR W/PAROMOMYCIN & VANCOM, Substantially Equivalent on 1982-12-03. Applicant: Granite Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Granite Diagnostics, Inc.
Product code: Code JSI
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1982-10-22
Decision date: 1982-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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