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

SENSORMEDICS 4000 SERIES SLEEP SYSTEM

K Number: K915856 · Decision Oct 26, 1992
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
35
Applicant Total
26
Review Days
304

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Basic Information

Device Name
SENSORMEDICS 4000 SERIES SLEEP SYSTEM
K Number
K915856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sensor Medics Corp.
Date Received
December 27, 1991
Decision Date
October 26, 1992
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.

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Other Clearances by Sensor Medics Corp.

K Number Device Name
K032516 HIOX80 AEROSOL ADAPTER
K031745 INFANT FLOW PLUS INFANT CPAP SYSTEM WITH SIPAP FUNCTION
K031883 LYRA NASAL MASK
K030943 MODIFICATION TO HIOX
K022192 PEGASUS NASAL CPAP SYSTEM
K020665 HI-OX
K012085 SOMNO STAR & SERIES SLEEP SYSTEM
K012034 MODIFICATION TO: SIPAP INFANT NASAL CPAP CIRCUIT
K991972 INFANT FLOW SYSTEM
K984254 INFANT FLOW NCPAP MASKS
Search all 26 clearances from Sensor Medics Corp. →