AMBULARM— 510(k) K840295

Substantially Equivalent

Rigi Systems, Inc.

FDA 510(k) clearance K840295 for AMBULARM, Substantially Equivalent on 1984-05-07. Applicant: Rigi Systems, Inc.. Device class: 1.

Clearance details

Applicant: Rigi Systems, Inc.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1984-01-24
Decision date: 1984-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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