Ellman Intl., Inc.
Ellman Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2001.
Top product codes for Ellman Intl., Inc.
Recent clearances by Ellman Intl., Inc.
- K013255 — SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF
- K003126 — BIPOLAR TRIGGER-FLEX PROBE
- K001986 — SURGITRON IEC II
- K001407 — SURGITRON IEC II
- K001253 — SURGITRON IEC II
- K992382 — SURGITRON RADIOLASE
- K990146 — SURGITRON
- K980177 — SUGITRON MODEL: IEC
- K980170 — SURGITRON
- K972072 — SURGITRON MODEL FFPF-EMC
- K955176 — DENTO-SURGE
- K954718 — ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGE
- K955158 — SURGITRON
- K954703 — MEDI-FRIG
- K955167 — SURGITRON
Data sourced from openFDA. This site is unofficial and independent of the FDA.