Gradipore , Ltd.
FDA Regulatory Profile
Gradipore , Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 16, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K993332 | GRADIPLASMA LA HIGH, GRADIPLASMA LA LOW MODELS LAHP-1, LAHP-05, LALP-1, LALP-05 | February 16, 2000 |
| K992456 | GRADILEIDEN V TEST | December 21, 1999 |
| K922156 | LUCOR CONFIRMATORY REAGENT | April 6, 1993 |
| K903037 | LUPO-TEST REAGENT | December 17, 1990 |