Collaboration Live
by Philips Ultrasound, Inc. 2 variants
510(k) K201665
Collaboration Live is a Class II device made by Philips Ultrasound, Inc., cleared under FDA 510(k) K201665 on 15 Sep 2020, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK201665 | Date15 Sep 2020 | StatusActive |
Official records
- FDA 510(k) database K201665
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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