510(k) K023450
K023450 is an FDA 510(k) premarket notification submitted by Promex, Inc. for the device "BIOPSY SITE TISSUE MARKER DEVICE". The FDA issued a decision of Substantially Equivalent on December 19, 2002. The device falls under product code NEU (Marker, Radiographic, Implantable), a Class II device regulated under 21 CFR 878.4300. Promex, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 19, 2002
- Date Received
- October 15, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Marker, Radiographic, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4300
- Review Panel
- SU
- Submission Type