Cox-Uphuff Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K874276CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDERDecember 2, 1987
K874342LIGATURE CARRIER/PACKER, HYDROXYLAPATITENovember 13, 1987
K873470TEMPLATESeptember 8, 1987
K865056CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDERMay 22, 1987
K871200CUI NASAL SEPTUM BUTTONApril 15, 1987
K865033BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDERJanuary 12, 1987
K854339CUI CHIN SIZERNovember 15, 1985
K853945CUI RHINOPLASTY IMPLANTSOctober 18, 1985
K831566CUI MAMMARY PROTHESIS SIZERAugust 12, 1983
K813394DS-7 CLOSED WOUND SUCTION DRAIN SYSTEMJanuary 22, 1982
K802214COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEMOctober 23, 1980