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FDA 510(k) Applications Submitted by CORNEL M TOPALA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000197
01/21/2000
CORTEK CYSTOSCOPE
CORTEK ENDOSCOPY, INC.
K000198
01/21/2000
CORTEK ARTHROSCOPE
CORTEK ENDOSCOPY, INC.
K000199
01/21/2000
CORTEK MINI LAPAROSCOPE
CORTEK ENDOSCOPY, INC.
K000200
01/21/2000
CORTEK URETHEROSCOPE
CORTEK ENDOSCOPY, INC.
K000202
01/21/2000
CORTEK LAPAROSCOPES
CORTEK ENDOSCOPY, INC.
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