LF900
FDA 510(k) clearance K231437 · decided 2023-07-19
Clearance details
- K-number
- K231437
- Device name
- LF900
- Applicant
- Daesung Maref Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2023-05-17
- Decision date
- 2023-07-19
- Days to decision
- 63 days
- Clearance type
- Special
- Product code
- IRP
- Device class
- 2
- Regulation number
- 890.5650
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Gunpo-Si, KR
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Daesung Maref Co.
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.