Option ELITE Vena Cava Filter System (352506070E 352506100E)
FDA 510(k) clearance K242612 · decided 2024-09-10
Clearance details
- K-number
- K242612
- Device name
- Option ELITE Vena Cava Filter System (352506070E 352506100E)
- Applicant
- Argon Medical Devices, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2024-09-03
- Decision date
- 2024-09-10
- Days to decision
- 7 days
- Clearance type
- Special
- Product code
- DTK
- Device class
- 2
- Regulation number
- 870.3375
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Athens, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.