UNIFUSE Infusion System with Cooper Wire
FDA 510(k) clearance K202347 · decided 2020-09-15
Clearance details
- K-number
- K202347
- Device name
- UNIFUSE Infusion System with Cooper Wire
- Applicant
- AngioDynamics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2020-08-18
- Decision date
- 2020-09-15
- Days to decision
- 28 days
- Clearance type
- Special
- Product code
- QEY
- Device class
- 2
- Regulation number
- 870.5150
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Marlborough, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.