Cleared Traditional

K981844 - SLEEP MANAGEMENT SYSTEM

K981844 is an FDA 510(k) clearance for SLEEP MANAGEMENT SYSTEM, manufactured by Rmp, Inc.. The device is a Class 2 Neurology device with product code HCC cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K981844 · Rmp, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1998
Decision
73d
Days
Class 2
Risk

K981844 is an FDA 510(k) clearance for the SLEEP MANAGEMENT SYSTEM. Classified as Device, Biofeedback (product code HCC), Class II - Special Controls.

Submitted by Rmp, Inc. (Washington, US). The FDA issued a Cleared decision on August 7, 1998 after a review of 73 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5050 - the FDA neurology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Rmp, Inc. devices

FDA 510(k) Submission Details - K981844

510(k) Number K981844 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 1998
Decision Date August 07, 1998
Days to Decision 73 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 148d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HCC Device Classification - Class 2, Special Controls

Product Code HCC Device, Biofeedback
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5050
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Neurology devices follow this clearance model.

Regulatory Peers - HCC Device, Biofeedback

All 42
Devices cleared under the same product code (HCC) and FDA review panel - the closest regulatory comparables to K981844.
THE BAGNOLI-8 EMG SYSTEM
K990356 · Delsys, Inc. · Apr 1999
XYZ SYSTEM
K983550 · Bio-Monitoring International Corp. · Jan 1999
THE BAGNOLI-4 EMG SYSTEM
K981934 · Delsys, Inc. · Aug 1998
ULTRAMIND BIOFEEDBACK SYSTEM WITH DE-STRESS SOFTWARE
K980373 · Ultramind International , Ltd. · Apr 1998
MUSCLE RESPONSE MONITOR
K971400 · Enriching Your Life · Apr 1998
PHYSIOLOGICAL MONITORING & BIOFEEDBACK TRAINING DEVICE
K971708 · J & J Engineering, Inc. · Feb 1998