Olympus Critical Care Monitoring System

FDA 510(k) K963935 · Optical Sensors, Inc.

Substantially Equivalent

510(k) numberK963935

Submission

Device name
Olympus Critical Care Monitoring System
Applicant
Optical Sensors, Inc.
Eden Prairie, MN, US
Received
October 1, 1996
Decision date
January 23, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CCC – Analyzer, Gas, Carbon-Dioxide, Partial Pressure, Blood-Phase, Indwelling
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1150
Specialty
Anesthesiology

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K972314Paratrend 7 Neotrend Multiparameter/Sensor with Paratrend 7 Multiparameter Senior and…CCC · Traditional Diametrics Medical, Ltd.12/19/1997SE
K953893Paratrend 7 Intravascular Blood Gas Monitoring SystemCCC · Traditional Biomedical Sensors, Inc.11/04/1997SE
K961790Point-Of-Care Blood Gas Monitor SystemCCC · Traditional Optical Sensors, Inc.04/09/1997SE
K951094Point-Of-Care Arterial Blood Gas Monitoring SystemCCC · Traditional Optical Sensors, Inc.01/16/1996SE
K940188Paratrend 7 Satellite Intravascular Blood Gas Monitoring SystemCCC · Traditional Biomedical Sensors, Ltd.11/13/1995SE
K931185Sensicath Point-Of-Care Blood Gas Monitoring SysteCCC · Traditional Optical Sensors, Inc.10/21/1993SE
K901548Biomedical Sensors-Shiley BGM 4000 Intra Blood GasCCC · Traditional Shiley, Inc.01/14/1991SE
K891013Medtronic Intravascular Blood Gas MonitoringCCC · Traditional Medtronic Vascular08/02/1989SE

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K961790Point-Of-Care Blood Gas Monitor SystemCCC · Traditional 04/09/1997SE
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Questions and answers

When was Olympus Critical Care Monitoring System cleared by the FDA?

Olympus Critical Care Monitoring System (K963935) received a 510(k) decision of Substantially Equivalent on January 23, 1997, 114 days after the submission was received.

What is the product code of K963935?

The FDA product code is CCC – Analyzer, Gas, Carbon-Dioxide, Partial Pressure, Blood-Phase, Indwelling, a Class II (moderate risk) device regulated under 21 CFR 868.1150.