Hyperion, Inc.
Hyperion, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 25, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K022800 | VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM | November 25, 2002 |
| K013213 | HYPERION VISIQUANT ANA TEST KIT | June 4, 2002 |
| K935983 | MICROREADER 4 | December 9, 1994 |
| K913809 | HY-PREP SYSTEM | January 15, 1992 |
| K873138 | MICRO-READER II | September 14, 1987 |
| K864060 | MICRO-READER | November 28, 1986 |
| K855149 | COMPUTING SPECTROPHOTOMETER BIO-CHEMISTRY ANALYZER | February 11, 1986 |
| K834071 | LYMPHANGIOGRAPHY SET SPECIAL 30G | January 25, 1984 |