FLEX ARM BE 122, CLAMP 122-27— 510(k) K770631

Name: FDA 510(k) clearance K770631
Creator: U.S. Food and Drug Administration
Published: 1977-05-23

Substantially Equivalent

Instrumentation Industries, Inc.

FDA 510(k) clearance K770631 for FLEX ARM BE 122, CLAMP 122-27, Substantially Equivalent on 1977-05-23. Applicant: Instrumentation Industries, Inc.. Device class: 1.

Clearance details

Applicant: Instrumentation Industries, Inc.
Product code: Code JAY
Device class: Class 1
Regulation: 21 CFR 868.5280
Advisory panel: Anesthesiology
Date received: 1977-04-04
Decision date: 1977-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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