Philips VSC-MEDlib
FDA 510(k) clearance K242001 · decided 2025-04-04
Clearance details
- K-number
- K242001
- Device name
- Philips VSC-MEDlib
- Applicant
- Philips Medical Systems Nederland B.V.
- Decision
- Substantially Equivalent
- Date received
- 2024-07-09
- Decision date
- 2025-04-04
- Days to decision
- 269 days
- Clearance type
- Traditional
- Product code
- BZQ
- Device class
- 2
- Regulation number
- 868.2375
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Eindhoven, NL
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.