Zee Medical Products Co., Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K823501 | ZEE SPHYGMOMANOMETER | January 21, 1983 |
| K813156 | ULTRA-WIDE SAFETY SPECTACLE FRAME | December 14, 1981 |
| K813016 | ZEE TRACTION SPLINT | November 24, 1981 |
| K812814 | ZEE SURGICAL INSTRUMENTS | November 6, 1981 |
| K812564 | ZEE LIFE SUPPORT AIR PANTS | October 23, 1981 |
| K812342 | ZEE EXTRICATION DEVICE | September 21, 1981 |
| K812284 | ZEE ELECTRODE-GEL | September 8, 1981 |
| K812022 | ZEE MANUAL RESUSCITATOR | July 31, 1981 |