PLEASCENT OR FORMA-SCENT— 510(k) K802506

Name: FDA 510(k) clearance K802506
Creator: U.S. Food and Drug Administration
Published: 1980-11-12

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K802506 for PLEASCENT OR FORMA-SCENT, Substantially Equivalent on 1980-11-12. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code IGG
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1980-10-15
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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