UNIVERSALLY ADJUSTABLE ARMBOARD— 510(k) K882524

Name: FDA 510(k) clearance K882524
Creator: U.S. Food and Drug Administration
Published: 1988-07-08

Substantially Equivalent

Karlin Technology, Inc.

FDA 510(k) clearance K882524 for UNIVERSALLY ADJUSTABLE ARMBOARD, Substantially Equivalent on 1988-07-08. Applicant: Karlin Technology, Inc.. Device class: 1.

Clearance details

Applicant: Karlin Technology, Inc.
Product code: Code BTX
Device class: Class 1
Regulation: 21 CFR 878.3910
Advisory panel: General, Plastic Surgery
Date received: 1988-06-17
Decision date: 1988-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marina Del Rey, CA, US

Download summary PDF View on FDA.gov ↗

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K882519 — X-RAY MARKER1988-08-09

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