LEGIONELLA DIFFERENTIATION DISK— 510(k) K834067

Substantially Equivalent

Remel Co.

FDA 510(k) clearance K834067 for LEGIONELLA DIFFERENTIATION DISK, Substantially Equivalent on 1984-01-03. Applicant: Remel Co.. Device class: 2.

Clearance details

Applicant: Remel Co.
Product code: Code GRO
Device class: Class 2
Regulation: 21 CFR 866.3300
Advisory panel: Microbiology
Date received: 1983-11-25
Decision date: 1984-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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