FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Hypnos (369054-200)

K Number: K250851 · Decision Dec 14, 2025
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
35
Applicant Total
12
Review Days
268

Basic Information

Device Name
Hypnos (369054-200)
K Number
K250851
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cadwell Industries, Inc.
Date Received
March 21, 2025
Decision Date
December 14, 2025
Product Code
OLZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OLZ), ordered by most recent decision date.

View all

Other Clearances by Cadwell Industries, Inc.

K Number Device Name
K242424 Bluebird Single-Use Respiratory Effort Belt
K230415 Cadwell Guardian
K201819 Cadwell Apollo System
K192624 ApneaTrak
K190760 Cadwell Bolt Software
K181466 Cadwell Zenith System
K180269 Cadwell Apollo System
K162199 Cascade IOMAX Intraoperative Monitor
K162383 Cadwell Sierra Summit, Cadwell Sierra Ascent
K161027 Cadwell AmpliScan
Search all 12 clearances from Cadwell Industries, Inc. →