FDA 510(k) Applications Submitted by SUSAN SMITH

FDA 510(k) Number Submission Date Device Name Applicant
K903412 07/30/1990 STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR. STORZ INSTRUMENT CO.
K904616 10/11/1990 STORZ ULTRA-SOURCE HIGH OUTPUT ILLUMINATOR STORZ INSTRUMENT CO.
K905376 11/30/1990 STORZ S6000 LIGHT SOURCE STORZ INSTRUMENT CO.
K022345 07/19/2002 AUTOPULSE RESUSCITATION SYSTEM REVIVANT CORP.
K973789 10/06/1997 NORIAN CRANIAL REPAIR SYSTEM (CRS)BONE CEMENT- 5CC KIT, NORIAN CRANIAL REPAIR SYSTEM (CRS) BONE CEMENT- 10CC NORIAN CORP.


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