GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSER— 510(k) K030574

Name: FDA 510(k) clearance K030574
Creator: U.S. Food and Drug Administration
Published: 2003-08-21

Substantially Equivalent

Glustitch, Inc.

FDA 510(k) clearance K030574 for GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSER, Substantially Equivalent on 2003-08-21. Applicant: Glustitch, Inc.. Device class: 1.

Clearance details

Applicant: Glustitch, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2003-02-24
Decision date: 2003-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Delta, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.