FDA Product Code
FDA Product Code DWQ — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Cardiovascular
- 21 CFR Citation
- 870.4885
510(k) Clearances — 8 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K212894 | PhasTIPP | LeMaitre Vascular, Inc. | 2022-03-31 | Traditional | PDF ↗ |
| K041453 | SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 | Smith & Nephew, Inc. | 2004-07-22 | Traditional | PDF ↗ |
| K032387 | TRIVEX SYSTEM | Smith & Nephew, Inc. | 2003-10-29 | Traditional | PDF ↗ |
| K905528 | URESIL VALVE CUTTER | Uresil Corp. | 1991-04-18 | Traditional | PDF ↗ |
| K904507 | PILLING BRUSH VALVULOTOME | Pilling Co. | 1991-03-01 | Traditional | PDF ↗ |
| K885046 | INSITUCAT VALVE STRIPPER | Aesculap Instruments Corp. | 1990-02-28 | Traditional | PDF ↗ |
| K872157 | HALL VEIN STRIPPER | Solco Basle, Inc. | 1987-07-07 | Traditional | PDF ↗ |
| K811910 | VEIN-TRAP TM | Atrium Medical Corp. | 1981-07-20 | Traditional | PDF ↗ |
Product code DWQ · Class II · Cardiovascular. Data: openFDA.