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PHYSIO-CONTROL RESUMES PRODUCTION

 REDMOND, Wash., May 19 /PRNewswire/ -- Physio-Control Corp. announced today it will resume shipment of its LIFEPAK(R) 10 defibrillator/monitor. The announcement follows a re-inspection by the FDA of the company's documentation, processes and procedures.
 Company officials say the LIFEPAK 10 defibrillator/monitor will be available for distribution shortly. It is anticipated production of the device will reach full volume during third quarter 1993. The company expects to resume shipment of its LIFEPAK 9 product line and LIFEPAK 300 automatic advisory defibrillator later this year.
 In mid-1992, Physio-Control voluntarily suspended shipping LIFEPAK products following an FDA biennial inspection in which the agency made observations with respect to certain federal manufacturing regulations. The observations related to documentation and manufacturing regulations and procedures. Last July the company signed an agreement that stipulated Physio-Control must satisfactorily undergo re-inspection by the FDA prior to resuming operations.
 Based in Redmond, Physio-Control designs, develops and manufactures defibrillator/pacemakers for emergency medical providers.
 -0- 5/19/93
 /CONTACT: Sandra Higgins of Physio-Control, 206-867-4574/


CO: Physio-Control ST: Washington IN: MTC SU:

LM-AL -- SE005 -- 0253 05/19/93 11:28 EDT
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Publication:PR Newswire
Date:May 19, 1993
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