FDA 510(k) Applications for Medical Device Product Code "HDA"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K092827 | DIMEDA INSTRUMENTE GMBH | DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX | 01/08/2010 |
K100517 | INSTRUMED INTERNATIONAL, INC. | INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXX | 04/29/2010 |
K013747 | TEKNO MEDICAL OPTIK-CHIRURGIE GMBH & CO. | TEKNO-MEDICAL OBSTETRICAL FORCEPS | 02/11/2002 |