IDS RAPID E PLUS SYSTEM— 510(k) K852110

Name: FDA 510(k) clearance K852110
Creator: U.S. Food and Drug Administration
Published: 1985-06-04

Substantially Equivalent

Innovative Diagnostic Systems, Inc.

FDA 510(k) clearance K852110 for IDS RAPID E PLUS SYSTEM, Substantially Equivalent on 1985-06-04. Applicant: Innovative Diagnostic Systems, Inc.. Device class: 1.

Clearance details

Applicant: Innovative Diagnostic Systems, Inc.
Product code: Code JSS
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1985-05-15
Decision date: 1985-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, US

Download summary PDF View on FDA.gov ↗

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