StaClear Syringe (3 models)— 510(k) K251849
Substantially EquivalentStaclear, Inc.
FDA 510(k) clearance K251849 for StaClear Syringe (3 models), Substantially Equivalent on 2025-11-21. Applicant: Staclear, Inc.. Device class: 2.
Clearance details
- Device name as filed
- StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL)
- Applicant
- Staclear, Inc.
- Product code
- Code QLY
- Device class
- Class 2
- Regulation
- 21 CFR 880.5860
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raleigh, NC, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.