BE #16 - MANIFOLD— 510(k) K823481

Name: FDA 510(k) clearance K823481
Creator: U.S. Food and Drug Administration
Published: 1982-12-22

Substantially Equivalent

Instrumentation Industries, Inc.

FDA 510(k) clearance K823481 for BE #16 - MANIFOLD, Substantially Equivalent on 1982-12-22. Applicant: Instrumentation Industries, Inc.. Device class: 1.

Clearance details

Applicant: Instrumentation Industries, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1982-11-23
Decision date: 1982-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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