PILOT TUBE REPAIR KIT— 510(k) K973755

Name: FDA 510(k) clearance K973755
Creator: U.S. Food and Drug Administration
Published: 1997-12-17

Substantially Equivalent

Instrumentation Industries, Inc.

FDA 510(k) clearance K973755 for PILOT TUBE REPAIR KIT, Substantially Equivalent on 1997-12-17. Applicant: Instrumentation Industries, Inc.. Device class: 2.

Clearance details

Applicant: Instrumentation Industries, Inc.
Product code: Code BSK
Device class: Class 2
Regulation: 21 CFR 868.5750
Advisory panel: Anesthesiology
Date received: 1997-10-02
Decision date: 1997-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethel Park, PA, US

Download summary PDF View on FDA.gov ↗

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