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

MASIMO SET MS-1 PULSE OXIMETER & THE LNOP SERIES OF SENSORS & CABLES

K Number: K962603 · Decision Feb 6, 1997
Classifications
1
FEI Numbers
403
Registration Numbers
403
Same Product Code
711
Applicant Total
28
Review Days
219

Basic Information

Device Name
MASIMO SET MS-1 PULSE OXIMETER & THE LNOP SERIES OF SENSORS & CABLES
K Number
K962603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MASIMO CORP.
Date Received
July 2, 1996
Decision Date
February 6, 1997
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DQA Oximeter

Similar 510(k) Clearances

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Other Clearances by MASIMO CORP.

K Number Device Name
K041815 LNCS OXIMETRY SENSORS
K041204 NC SP02 ADAPTER CABLE
K040259 MASIMO SET INTELLIVUE PULSE OXIMETER MODULE
K033998 MASIMO SET RAD-5V PULSE OXIMETER, MODEL RAD-5V
K040214 MODIFICATION TO: MASIMO SET RADICAL PULSE OXIMETER WITH SATSHARE AND LNOP SERIES OF SENSORS AND CABLES
K032551 MASIMO LNOP-TF-I RESUABLE TRANSFLECTANCE SENSOR
K033296 MASIMO SET RAD-5 PULSE OXIMETER, MODEL RAD-5; MASIMO SET RAD-5V PULSE OXIMETER, MODEL RAD-5V
K033349 AC-1 SP02 ADAPTOR CABLE, MODEL AC-1
K033298 SPO2.COM OXIMETRY SENSORS, MULTIPLE MODELS
K031330 MODIFICATION TO MASIMO SET RADICAL PULSE OXIMETER WITH SATSHARE AND LNOP SERIES OF SENSORS AND CABLES
Search all 28 clearances from MASIMO CORP. →