INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050— 510(k) K891005

Name: FDA 510(k) clearance K891005
Creator: U.S. Food and Drug Administration
Published: 1989-05-11

Substantially Equivalent

3M Company

FDA 510(k) clearance K891005 for INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050, Substantially Equivalent on 1989-05-11. Applicant: 3M Company. Device class: 2.

Clearance details

Applicant: 3M Company
Product code: Code FPK
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 1989-02-28
Decision date: 1989-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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