ClearanceBrief
Company ยท US

Harris-Lake, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1977. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KDPRegulator, Vacuum2
BTICompressor, Air, Portable1
BTTHumidifier, Respiratory Gas, (Direct Patient Interface)1
BZEHeater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer1
CAXFlowmeter, Tube, Thorpe, Back-Pressure Compensated1
GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 3, 1977K761294RESPIRATORY BLOWER
Harris-Lake, Inc.
BTI
Jan 3, 1977K761293RESPIRATORY HUMIDIFIER
Harris-Lake, Inc.
BTT
Dec 30, 1976K761295RESP. AIR TEMP. CONTROL & HAZARD MON.
Harris-Lake, Inc.
BZE
Oct 27, 1976K760333JAR, COLLECTOR FOR SUCTION SYSTEMS
Harris-Lake, Inc.
GCX
Aug 4, 1976K760317REGULATORS, HIGH SUCTION
Harris-Lake, Inc.
KDP
Aug 4, 1976K760316REGULATORS, LOW SUCTION
Harris-Lake, Inc.
KDP
Aug 4, 1976K760314FLOWMETER, OXYGEN
Harris-Lake, Inc.
CAX

Latest recalls

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