EndoRotor
FDA 510(k) clearance K170120 · decided 2017-04-18
Clearance details
- K-number
- K170120
- Device name
- EndoRotor
- Applicant
- Interscope, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2017-01-13
- Decision date
- 2017-04-18
- Days to decision
- 95 days
- Clearance type
- Traditional
- Product code
- PTE
- Device class
- 2
- Regulation number
- 884.1690
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Worchester, MA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control (K181127) | Interscope, Inc. | 2019-01-03 |
Recalls involving this device
No recalls on record reference this clearance.