Interscope, Inc.
Interscope, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 23, 2020.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| DEN200016 | EndoRotor Device | December 23, 2020 |
| K190715 | EndoRotor Console, EndoRotor Catheter, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Roll | December 13, 2019 |
| K181127 | EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foo | January 3, 2019 |
| K170120 | EndoRotor | April 18, 2017 |