FDA 510(k) Applications Submitted by GYNEX CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K980237 01/23/1998 GYNEX ENDOSPECULUM GYNEX CORP.
K980238 01/23/1998 GYNEX EXTENDED REACH NEEDLE GYNEX CORP.
K980247 01/23/1998 GYNEX IRIS HOOK, GYNEX ANGLE HOOK, GYNEX EMMETT TENACULUM GYNEX CORP.
K982739 08/06/1998 GYNEX ELECTRODES GYNEX CORP.
K061306 05/10/2006 CO-1000 COLPOSCOPE, MULTIPLE GYNEX CORP.


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