Schneider Intl., Ltd.
Minneapolis, MN, US
Schneider Intl., Ltd. appears in FDA device records in Minneapolis, MN. FDA records list 22 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 22
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 22 510(k) clearances for Schneider Intl., Ltd. between 1989 and 1995. The busiest year on record is 1991, with 7. The most recent is 1995, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 1 |
| 1990 | 4 |
| 1991 | 7 |
| 1992 | 5 |
| 1993 | 4 |
| 1995 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K925406 | BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM | FGE | Substantially Equivalent | |
| K931577 | SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI | DQX | Substantially Equivalent | |
| K926271 | SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO | LIT | Substantially Equivalent | |
| K926003 | SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETER | DQO | Substantially Equivalent | |
| K925804 | SCHNEIDER HYDRO-SIL GUIDEWIRE | DQX | Substantially Equivalent | |
| K924591 | SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER | DQY | Substantially Equivalent | |
| K921856 | TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH. | LIT | Substantially Equivalent | |
| K921943 | SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BAL | LIT | Substantially Equivalent | |
| K920157 | SCHNEIDER 8 FR. STAMINA(TM) GUIDING CATHETER | DXY | Substantially Equivalent | |
| K915349 | PTA BALLOON CATHETER | LIT | Substantially Equivalent | |
| K914009 | SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER | DQO | Substantially Equivalent | |
| K913297 | SCHNEIDER MATCH-35(TM) PERCU TRANS ANGIOPLAS CATH | LIT | Substantially Equivalent | |
| K912156 | SCHNEIDER MAGNUM PERIPHERAL RECANAL GUIDEWIRE | DQX | Substantially Equivalent | |
| K912317 | SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO PTA CATH | LIT | Substantially Equivalent | |
| K911547 | MAGNUM-MEIER RECANALIZATION GUIDEWIRE | DQX | Substantially Equivalent | |
| K911196 | SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) | LIT | Substantially Equivalent | |
| K910259 | SCHNEIDER MAGNARAIL PROBING CATHETER | DQO | Substantially Equivalent | |
| K902587 | SCHNEIDER MONORAIL-GEX(TM) GUIDEWIRE EXCHANGE CATH | DQY | Substantially Equivalent | |
| K902091 | SCHNEIDER MONORAIL(TM) SOFTRAC-PTA(TM) CATHETER | LIT | Substantially Equivalent | |
| K897082 | SCHNEIDER SIDEKICK MONORAIL Y-CONNECTOR | DQY | Substantially Equivalent | |
| K896741 | SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH. | DQO | Substantially Equivalent | |
| K885180 | EXPANDABLE BILIARY STENT ENDOPROSTHESIS | FGE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain