SLEEP MANAGEMENT SYSTEM— 510(k) K981844

Substantially Equivalent

Rmp, Inc.

FDA 510(k) clearance K981844 for SLEEP MANAGEMENT SYSTEM, Substantially Equivalent on 1998-08-07. Applicant: Rmp, Inc.. Device class: 2.

Clearance details

Applicant: Rmp, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1998-05-26
Decision date: 1998-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.