K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH— 510(k) K970441

Name: FDA 510(k) clearance K970441
Creator: U.S. Food and Drug Administration
Published: 1997-05-09

Substantially Equivalent

Medi-Flex Hospital Products, Inc.

FDA 510(k) clearance K970441 for K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH, Substantially Equivalent on 1997-05-09. Applicant: Medi-Flex Hospital Products, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Flex Hospital Products, Inc.
Product code: Code FPX
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 1997-02-05
Decision date: 1997-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

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