Medi Nuclear Corp., Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K082541 | HEALTHLINE MEDICATOR / REDINEB AEROSOL DRUG DELIVERY SYSTEM | November 26, 2008 |
| K080969 | HEALTHLINE REDI-NEB MEDICATION NEBULIZER, MODEL RN-510 | July 25, 2008 |
| K080657 | NEB-90 LARGE VOLUME MEDICATION NEBULIZER | June 30, 2008 |
| K915075 | NEBULIZER (DIRECT PATIENT INTERFACE) | July 16, 1992 |
| K865107 | AERO-VENT AEROSOL UNIT | October 20, 1987 |
| K865093 | SAFE-T-SHIELD MOUTHPIECE | January 15, 1987 |
| K863996 | MODEL XE-103 XENON/MASTER II | November 4, 1986 |
| K813379 | RADIONUCLIDE DOSE CALIBRATOR | January 22, 1982 |
| K810819 | MEDI/NUCLEAR #XE-102 XENON/MASTER | April 14, 1981 |