FDA 510(k) Applications for Medical Device Product Code "KLK"
(Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia)

FDA 510(k) Number Applicant Device Name Decision Date
K924709 AIR-SHIELDS, INC. SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETE 01/17/1996
K003943 LINDE MEDICAL SENSORS AG MICROGAS 7650 TRANSCUTANEOUS MONITOR 05/04/2001
K991644 LINDE MEDICAL SENSORS AG MICROGAS 7650 TRANSCUTANEOUS MONITOR 05/21/1999
K980287 SIEMENS MEDICAL SOLUTIONS USA, INC. SIEMENS SC9000/SC9015 TCP02/C02 MODULE 08/12/1998


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