Coolfase
FDA 510(k) clearance K250852 · decided 2025-10-16
Clearance details
- K-number
- K250852
- Device name
- Coolfase
- Applicant
- Asterasys Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2025-03-21
- Decision date
- 2025-10-16
- Days to decision
- 209 days
- Clearance type
- Traditional
- Product code
- GEI
- Device class
- 2
- Regulation number
- 878.4400
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Seoul, KR
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Asterasys 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.