FDA Product Code
FDA Product Code DWO — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4800
510(k) Clearances — 11 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K933364 | PROMED BIOPSY NEEDLE | Vlv Associates, Inc. | 1994-02-15 | Traditional | PDF ↗ |
| K921418 | ULTRA-CORE BIOPSY NEEDLES | Medical Device Technologies, Inc. | 1992-06-19 | Traditional | PDF ↗ |
| K913815 | AUTOMATED BIOPSY DEVICE, MODIFICATION | Hart Enterprises, Inc. | 1991-10-30 | Traditional | PDF ↗ |
| K890925 | MANAN BONE MARROW BIOPSY NEEDLE | Manan Medical Products, Inc. | 1989-04-11 | Traditional | PDF ↗ |
| K885145 | MEDSURG GREENE NEEDLE | Medsurg Industries, Inc. | 1989-03-14 | Traditional | PDF ↗ |
| K885149 | NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE | Hart Enterprises, Inc. | 1989-01-26 | Traditional | PDF ↗ |
| K882013 | SOFT TISSUE BIOPSY DEVICE | Ocean Medical Products, Ltd. | 1988-06-15 | Traditional | PDF ↗ |
| K874585 | ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE | Angiomed U.S., Inc. | 1987-12-02 | Traditional | PDF ↗ |
| K872597 | FINE NEEDLE ASPIRATION BIOPSY SYSTEM-PROSTATE | Dianon Systems, Inc. | 1987-07-28 | Traditional | PDF ↗ |
| K853312 | ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES | Argon Medical Corp. | 1985-09-12 | Traditional | PDF ↗ |
| K820269 | RNG SERIES ULTRASOUND NEEDLE/CATH. GDS | CIVCO Medical Instruments Co., Inc. | 1982-03-23 | Traditional | PDF ↗ |
Product code DWO · Class I · General, Plastic Surgery. Data: openFDA.