3M MULTI-ALLERGEN IGE FASTSCREEN(TM) S8— 510(k) K900244

Name: FDA 510(k) clearance K900244
Creator: U.S. Food and Drug Administration
Published: 1990-02-21

Substantially Equivalent

3M Company

FDA 510(k) clearance K900244 for 3M MULTI-ALLERGEN IGE FASTSCREEN(TM) S8, Substantially Equivalent on 1990-02-21. Applicant: 3M Company. Device class: 2.

Clearance details

Applicant: 3M Company
Product code: Code DGC
Device class: Class 2
Regulation: 21 CFR 866.5510
Advisory panel: Immunology
Date received: 1990-01-17
Decision date: 1990-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

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