Biotrine Corp.
FDA Regulatory Profile
Biotrine Corp. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 11, 1992.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K915060 | ASTECH HOME PEAK FLOW METER | Sep 11, 1992 |
| K883704 | MULTIICHALLENGE NEBULIZER SYSTEM | Nov 28, 1988 |
| K863134 | MULTISPIRO SA/100 | Dec 15, 1986 |
| K844226 | B-1000 | Nov 20, 1984 |
| K813414 | PEAK FLOW MONITOR | Dec 31, 1981 |
| K812825 | FLO-COR I | Oct 26, 1981 |