SYRINGE 500BC BE #7000— 510(k) K830898

Name: FDA 510(k) clearance K830898
Creator: U.S. Food and Drug Administration
Published: 1983-05-16

Substantially Equivalent

Instrumentation Industries, Inc.

FDA 510(k) clearance K830898 for SYRINGE 500BC BE #7000, Substantially Equivalent on 1983-05-16. Applicant: Instrumentation Industries, Inc.. Device class: 1.

Clearance details

Applicant: Instrumentation Industries, Inc.
Product code: Code BXW
Device class: Class 1
Regulation: 21 CFR 868.1870
Advisory panel: Anesthesiology
Date received: 1983-03-21
Decision date: 1983-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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