Kapp Surgical Instrument, Inc.
Kapp Surgical Instrument, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jan 28, 2021.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K200289 | Michler-Kapp Cardiovascular Vent Catheter | Jan 28, 2021 |
| K072216 | KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536 | Nov 9, 2007 |
| K050384 | KAPP BARI-RING, MODEL KS-BR-2005 | Jan 13, 2006 |
| K050655 | MONDEAL RADIUS HO SYSTEM, MODEL KS-MR-2005 | Aug 8, 2005 |
| K050657 | MONDEAL CONTOUR HO SYSTEM | Aug 8, 2005 |
| K033930 | KAPP CUSTOM ULNAR HEAD WRIST IMPLANT | Jul 28, 2004 |
| K030237 | KAPP CUSTOM RADIAL HEAD ELBOW IMPLANT | Aug 29, 2003 |
| K844177 | COSGROVE MITRAL VALVE RETRACTOR | Nov 8, 1984 |
| K843368 | KAPP SPINAL BUTTON | Sep 12, 1984 |