Schneider Intl., Ltd.
Schneider Intl., Ltd. appears in FDA public data with 0 recalls, 22 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 11, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 22
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K925406 | BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM | January 11, 1995 |
| K931577 | SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI | June 23, 1993 |
| K926003 | SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETER | June 7, 1993 |
| K926271 | SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO | June 7, 1993 |
| K925804 | SCHNEIDER HYDRO-SIL GUIDEWIRE | February 12, 1993 |
| K924591 | SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER | December 8, 1992 |
| K921856 | TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH. | July 21, 1992 |
| K921943 | SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BAL | June 17, 1992 |
| K920157 | SCHNEIDER 8 FR. STAMINA(TM) GUIDING CATHETER | March 16, 1992 |
| K915349 | PTA BALLOON CATHETER | February 11, 1992 |
| K914009 | SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER | December 6, 1991 |
| K913297 | SCHNEIDER MATCH-35(TM) PERCU TRANS ANGIOPLAS CATH | October 10, 1991 |
| K912156 | SCHNEIDER MAGNUM PERIPHERAL RECANAL GUIDEWIRE | September 6, 1991 |
| K912317 | SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO PTA CATH | August 22, 1991 |
| K911547 | MAGNUM-MEIER RECANALIZATION GUIDEWIRE | July 5, 1991 |
| K911196 | SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) | June 10, 1991 |
| K910259 | SCHNEIDER MAGNARAIL PROBING CATHETER | April 18, 1991 |
| K902587 | SCHNEIDER MONORAIL-GEX(TM) GUIDEWIRE EXCHANGE CATH | December 3, 1990 |
| K902091 | SCHNEIDER MONORAIL(TM) SOFTRAC-PTA(TM) CATHETER | September 26, 1990 |
| K897082 | SCHNEIDER SIDEKICK MONORAIL Y-CONNECTOR | March 6, 1990 |