Ellman Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Known Names

ellman int'l, ellman intl

Recent 510(k) Clearances

K-NumberDeviceDate
K013255SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RFNovember 7, 2001
K003126BIPOLAR TRIGGER-FLEX PROBEApril 11, 2001
K001986SURGITRON IEC IISeptember 27, 2000
K001407SURGITRON IEC IIJuly 24, 2000
K001253SURGITRON IEC IIMay 26, 2000
K992382SURGITRON RADIOLASEOctober 14, 1999
K990146SURGITRONMarch 17, 1999
K980177SUGITRON MODEL: IECJuly 7, 1998
K980170SURGITRONJune 29, 1998
K972072SURGITRON MODEL FFPF-EMCJune 19, 1997
K955176DENTO-SURGEApril 15, 1996
K954718ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGEFebruary 29, 1996
K955158SURGITRONFebruary 9, 1996
K954703MEDI-FRIGFebruary 8, 1996
K955167SURGITRONFebruary 8, 1996