Company ยท US
Ellman Intl., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 2001. Name variants (Inc, Corp, punctuation) are merged.
15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 7, 2001 | K013255 | SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF Ellman Intl., Inc. | GEI |
| Apr 11, 2001 | K003126 | BIPOLAR TRIGGER-FLEX PROBE Ellman Intl., Inc. | GEI |
| Sep 27, 2000 | K001986 | SURGITRON IEC II Ellman Intl., Inc. | GEI |
| Jul 24, 2000 | K001407 | SURGITRON IEC II Ellman Intl., Inc. | GEI |
| May 26, 2000 | K001253 | SURGITRON IEC II Ellman Intl., Inc. | GEI |
| Oct 14, 1999 | K992382 | SURGITRON RADIOLASE Ellman Intl., Inc. | GEI |
| Mar 17, 1999 | K990146 | SURGITRON Ellman Intl., Inc. | GEI |
| Jul 7, 1998 | K980177 | SUGITRON MODEL: IEC Ellman Intl., Inc. | GEI |
| Jun 29, 1998 | K980170 | SURGITRON Ellman Intl., Inc. | GEI |
| Jun 19, 1997 | K972072 | SURGITRON MODEL FFPF-EMC Ellman Intl., Inc. | GEI |
| Apr 15, 1996 | K955176 | DENTO-SURGE Ellman Intl., Inc. | EKZ |
| Feb 29, 1996 | K954718 | ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGE Ellman Intl., Inc. | HEE |
| Feb 9, 1996 | K955158 | SURGITRON Ellman Intl., Inc. | HQR |
| Feb 8, 1996 | K955167 | SURGITRON Ellman Intl., Inc. | GEI |
| Feb 8, 1996 | K954703 | MEDI-FRIG Ellman Intl., Inc. | GEH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||