VasQ
FDA 510(k) clearance K240119 · decided 2024-02-16
Clearance details
- K-number
- K240119
- Device name
- VasQ
- Applicant
- Laminate Medical Technologies , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2024-01-16
- Decision date
- 2024-02-16
- Days to decision
- 31 days
- Clearance type
- Special
- Product code
- QVQ
- Device class
- 2
- Regulation number
- 870.4600
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Tel Aviv, IL
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Laminate Medical Technologies
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.
| Record | Firm | Date |
|---|---|---|
| VasQ (DEN220026) | Laminate Medical Technologies , Ltd. | 2023-09-26 |
Recalls involving this device
No recalls on record reference this clearance.