MJG — Device, Percutaneous, Biopsy Class I
FDA Device Classification
Classification Details
- Product Code
- MJG
- Device Class
- Class I
- Regulation Number
- 878.4800
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K080674 | pajunk gmbh medizintechnologie | PAJUNK'S PRIMOCUT DISPOSABLE BIOPSY SYSTEM | May 9, 2008 |
| K070836 | clevex | EXICLIP EXCS-M | April 20, 2007 |
| K983647 | sts biopolymers | ECHO-COAT ULTRASOUND NEEDLES | January 20, 1999 |
| K955683 | contour fabricators of florida | RNS STERILE, DISPOSABLE BREAST BIOPSY/LOCALIZATION TRAY | February 1, 1996 |
| K933324 | nhr | SKIN BIOPSY DEVICE | March 31, 1994 |
| K925870 | bip usa | SPACER | May 19, 1993 |
| K922919 | buckman co | DYNACYT BIOPSY ASPIRATION DEVICE | March 31, 1993 |