FDA 510(k) K993953 OVES CERVICAL CAP

Device Classification Name: Cap, Cervical
510(k) Number: K993953
Device Name: OVES CERVICAL CAP
Applicant: VEOS LTD.
Regulation Number: 884.5250
Classification Product Code: HDR  
Date Received: 11/22/1999
Decision Date: 03/21/2000
Decision: SE - With Limitations (SESU)
Regulation Medical Specialty: Obstetrics/Gynecology
Type: Traditional

Total Pages: 129
Fully Redacted Pages: 91
Content Pages: 38 (total pages minus fully redacted pages)