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510(k) Data Aggregation
K Number
K123946Device Name
WARMAIR MODEL 135 HYPERTHERMIA SYSTEM INCLUDING FILTEREDFLO BLANKETS
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC
Date Cleared
2013-01-17
(27 days)
Product Code
DWJ
Regulation Number
870.5900Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The WarmAir® 135 patient warming system is intended to prevent hypothermia and/or reduce cold discomfort before, during, and after surgical procedures. The thermal regulating system is used to raise a patient's temperature and/or maintain a desired patient temperature through convective heat transfer from the controller to a warm-airheated blanket. The single-patient use blankets transfer the thermal energy to adult, pediatric or neonate patients to obtain/maintain normal body temperature. It is intended for use by appropriately trained healthcare professionals in clinical environments.
Device Description
The WarmAir 135 Hyperthermia System is a patient temperature management device which provides forced air warmed by the controller to a blanket that is placed over or under adult, pediatric or neonatal patients in order to warm them. The heated air is blown through connecting flexible hose to a disposable blanket to provide patient therapy by the means of warmed air.
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K Number
K122813Device Name
HEMOTHERM MODEL 400CE COOLER/HEATER SYSTEM
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC.
Date Cleared
2012-12-18
(96 days)
Product Code
DWC
Regulation Number
870.4250Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Hemotherm Dual Reservoir Cooler/Heater is used to lower, maintain, or raise the temperature of the water flowing through a Blood Oxygenator/Heat Exchanger that is used to cool or warm blood during cardiopulmonary bypass procedures lasting six hours or less. The Hemotherm Dual Reservoir Cooler/Heater may also be used with a hyper/hypothermia blanket under the patient to provide warming through conductive heat transfer.
Device Description
The Hemotherm® Model 400CE Cooler/Heater System is a dual reservoir, water recirculating device that supplies temperature controlled water to a heat exchanger. The device, in conjunction with a heat exchanger, is used to warm or cool the blood that enters and exits a blood heat exchanger for adult, pediatric or infant patients. The device uses conductive heat transfer. When ordered by the health care professional, the device can also simultaneously supply temperature controlled water to a blanket to provide additional patient re-warming therapy. If the blanket is used at the same time as the heat exchanger, the blanket is supplied the same water that circulates to the heat exchanger.
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K Number
K121669Device Name
WARMAIR MODEL 135 HYPERTHERMIA SYSTEM (CONTROLLER AND BLANKETS)
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC.
Date Cleared
2012-07-03
(27 days)
Product Code
DWJ
Regulation Number
870.5900Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The WarmAir® 135 patient warming system is intended to prevent hypothermia and/or reduce cold discomfort before, during, and after surgical procedures. The thermal regulating system is used to raise a patient's temperature and/or maintain a desired patient temperature through convective heat transfer from the controller to a warm-airheated blanket. The single-patient use blankets transfer the thermal energy to adult, pediatric or neonate patients to obtain/maintain normal body temperature. It is intended for use by appropriately trained healthcare professionals in clinical environments.
Device Description
The WarmAir 135 Hyperthermia System is a patient temperature management device which provides forced air warmed by the controller to a blanket that is placed over or under adult, pediatric or neonatal patients in order to warm them. The heated air is blown through connecting flexible hose to a disposable blanket to provide patient therapy by the means of warmed air.
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K Number
K120081Device Name
NORM-O-TEMP HYPERTHERMIA SYSTEM INCLIDING BLANKETS/PADS
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC.
Date Cleared
2012-02-17
(37 days)
Product Code
DWJ
Regulation Number
870.5900Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Norm-O-Temp® Model 111Z hyperthermia system is intended to prevent hypothermia during surgical procedures and to reduce cold discomfort before, during, and after a surgical procedure. The thermal regulating system is used to keep a patient comfortable by maintaining blanket/pad water temperature through conductive heat transfer. The water heated blankets transfer the thermal energy to adult, pediatric, and infant (includes neonates) patients to keep a patient at a comfortable temperature. The Norm-O-Temp system is composed of a heater, circulating pump, and blankets/pads. It is intended for use by appropriately trained healthcare professionals in clinical environments.
Device Description
The Cincinnati Sub-Zero Norm-O-Temp (Model 111Z) is a water re-circulating system providing either hyperthermia or normothermia treatment as determined by the health care provider. It is a total body hyperthermia system used to keep a patient comfortable by maintaining blanket/pad water temperature through conductive heat transfer. Water is heated and pumped from the device, through connecting flexible tubing, to disposable or reusable blankets/pads. The blankets/pads rest under, on top of and/or around the patient and are designed so that the water circulates through the blankets/pads and returns back to the device. The device is designed to operate based on the temperature of the circulating water. The system is used in Operating rooms, Post Anesthesia Care Units, Recovery rooms, Intensive Care Units, and Emergency Rooms with adult, pediatric and infant (including neonate) patients. The blankets/pads that are used with the Norm-O-Temp system are offered in a variety of sizes from large to small to meet the needs of the patients.
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K Number
K110104Device Name
BLANKETROL II HYPER-HYPOTHERMIA TEMPERATURE MANAGMENT SYSTEM
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC.
Date Cleared
2011-02-04
(22 days)
Product Code
DWJ
Regulation Number
870.5900Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Blanketrol II Model 222S Hyper-Hypothermia Temperature Management System is used to lower or to raise a patient's temperature and/or maintain a desired patient temperature through conductive heat transfer. The system is composed of a heater, a compressor, a circulating pump and blankets/pads.
Device Description
The Blanketrol II Model 222S is a water (liquid) recirculating device providing either hypothermia, hyperthermia or normothermia treatment as determined by the health care provider. Water is either heated or cooled depending on the need of the patient. The heated or cooled water is pumped through connecting flexible tubing to a disposable or reusable pad or blanket to provide patient therapy for a site specific external surface area or for whole body surface temperature therapy by the means of conductive heat transfer.
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K Number
K101148Device Name
WARM AIR MODEL 135 HYPERTHERMIA SYSTEM AND BLANKETS
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC
Date Cleared
2010-10-01
(161 days)
Product Code
DWJ
Regulation Number
870.5900Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The WarmAir® 135 patient warming system is intended to prevent hypothermia and/or reduce cold discomfort before, during, and after surgical procedures. The thermal regulating system is used to raise a patient's temperature and/or maintain a desired patient temperature through convective heat transfer from the controller to a warm-air-heated blanket. The single-patient use blankets transfer the thermal energy to adult, pediatric or neonate patients to obtain/maintain normal body temperature. It is intended for use by appropriately trained healthcare professionals in clinical environments.
Device Description
The WarmAir 135 Hyperthermia System is a patient temperature management device which provides forced air warmed by the controller to a blanket that is placed over or under adult, pediatric or neonatal patients in order to warm them. The heated air is blown through connecting flexible hose to a disposable blanket to provide patient therapy by the means of warmed air.
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K Number
K101589Device Name
BLANKETROL III, MODEL 233 AND COOLBLUE, MODEL 25-01 HYPER-HYPOTHERMIA SYSTEMS
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC.
Date Cleared
2010-09-20
(105 days)
Product Code
DWJ
Regulation Number
870.5900Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Blanketrol III Model 233 and CoolBlue Model 25-01 Hyper-Hypothermia Temperature Management Systems are used to lower or to raise a patient's temperature and/or maintain a desired patient temperature through conductive heat transfer. The system is composed of a heater, a compressor, a circulating pump and blankets/pads.
Device Description
The Blanketrol III/CoolBlue Hyper-Hypothermia System is a water (liquid) recirculating device providing either hypothermia, hyperthermia or normothermia treatment as determined by the health care provider. Water is either heated or cooled depending on the need of the patient. The heated or cooled water is pumped through connecting flexible tubing to a disposable or reusable pad or blanket to provide patient therapy for a site specific external surface area or for whole body surface temperature therapy by the means of conductive heat transfer.
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K Number
K072621Device Name
ESOPHAGEAL/RECTAL TEMPERATURE PROBE AND ESOPHAGEAL STETHOSCOPE WITH TEMPERATURE SENSOR
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC
Date Cleared
2007-12-13
(87 days)
Product Code
BZT
Regulation Number
868.1920Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Esophageal/Rectal Temperature Probe, Catalog Numbers 483M-9, 483M-12, and 491B: The CSZ sesphageal/rectal temperature probe is intended for use in routine continuous monitoring of the esophageal or medal temperature as an indicator or core body temperature. The probe is designed for placement in the esophagus or rectum.
Boohageal Stethoscope with Temperature Sensor, Catalog Numbers 493M-9, 493M-12, 493M-18, and 493M-24: The CSZ esophageal stethoscope with temperature sensor is intended for use when the esophageal caperature is continuously monitored along with the auscultation of the heart and lung sound as an indicator of core body temperature and cardio-pulmonary performance.
Device Description
Disposable Temperature Probes using thermistors as temperature sensors. The signal of the sensor s processed and displayed by the monitoring unit.
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K Number
K070339Device Name
DISPOSABLE TEMPERATURE PROBES/SENSORS AND INSTRUMENT CABLES
Manufacturer
CINCINNATI SUB-ZERO PRODUCTS, INC
Date Cleared
2007-09-26
(233 days)
Product Code
FLL
Regulation Number
880.2910Why did this record match?
Applicant Name (Manufacturer) :
CINCINNATI SUB-ZERO PRODUCTS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Skin Temperature Sensor (487M and 499B): The CSZ skin temperature sensor is intended for use in routine continuous monitoring skin temperature when the other sensors which might better reflect core body temperature are not indicated clinically. The sensor is designed for placement on the surface of the skin.
Tympanic Temperature Sensor (495M and 495M-P): The tympanic temperature sensor is intended for use in routine continuous monitoring tympanic temperature as an indicator of core body temperature when this type of measurement is clinically indicated.
Instrument Cables (4872MS and 4900B): The intended use of the instrument cable is to interconnect the disposable temperature sensor/probe with the temperature monitoring instrument.
Device Description
The basic component of these sensors is a resistance chip, which is sensitive to changes in temperature. The chip is in the form of "400" series thermistor connected to a lead wire and encapsulated in a PVC cup. At the end of the lead wires an insert molded connector or standard phone connector provides for the interconnection with the instrument cable.
These sensors are inserted in the structure that fits specific anatomy where the temperature is measured.
The skin sensor is placed on the surface of the skin and is a part of the foam enclosure which provides thermal insulation for more accurate temperature measurement.
The tympanic probe is designed for placement in proximity to the tympanic membrane, The probe incorporates a small foam tip for atraumatic insertion and a large compressible foam cylinder for securement and thermal insulation.
The distal end of the skin sensor and the tympanic sensor is terminated with a Molex or phone connector for interconnection with the instrument cable.
The probes are individually packaged in sterilizable bags. There are 20 probes per box and 10 boxes per shipping carton. Probes are ethylene oxide sterilized.
The following probes and cables are included in this 510k application:
Probes:
Skin Temperature Sensor (487M, 499B) Tympanic Temperature Sensor (495M, 495M-P) Cables (4872MS, 4900B)
These probes can be used with Smith's Level 1 TM-200 temperature/monitors or any other multi-channel patient monitor compatible with the "400" series thermistors or equivalent.
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