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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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