ClearanceBrief
Company ยท US

Caradyne, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2004. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CAPMonitor, Airway Pressure (Includes Gauge And/Or Alarm)2
BYEAttachment, Breathing, Positive End Expiratory Pressure1
BZDVentilator, Non-Continuous (Respirator)1
CCLAnalyzer, Gas, Oxygen, Gaseous-Phase1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 30, 2004K040862GUARDIAN NEONATE CPAP/HUMIDIFICATION SYSTEM
Caradyne, Ltd., IE
BZD
Mar 28, 2003K023565OXICHECK
Caradyne, Ltd.
CCL
Jun 22, 2000K000959CRITERION 60 OR PM 60
Caradyne, Ltd.
CAP
Jan 6, 2000K992101CRITERION 40 OR PM 40
Caradyne, Ltd.
CAP
Mar 9, 1999K982283WHISPERFLOW OXYGEN FLOW GENERATOR - ADJUSTABLE MODEL WF 8500 WHISPERFLOW OXYGEN FLOW GENERATOR - FIXED MODEL WF 8530 WH
Caradyne, Ltd.
BYE

Latest recalls

DateFirm and productCodeLinked 510(k)
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