The following data is part of a premarket notification filed by Schneider Intl., Ltd. with the FDA for Total Cross .021 Percut. Transluminal Angio. Cath..
| Device ID | K921856 |
| 510k Number | K921856 |
| Device Name: | TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH. |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | SCHNEIDER INTL., LTD. 5905 NATHAN LN. Plymouth, MN 55442 |
| Contact | Robert L Ullen |
| Correspondent | Robert L Ullen SCHNEIDER INTL., LTD. 5905 NATHAN LN. Plymouth, MN 55442 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-04-17 |
| Decision Date | 1992-07-21 |