StaClear Syringe— 510(k) K200242
Substantially EquivalentTribofilm Research, Inc.
FDA 510(k) clearance K200242 for StaClear Syringe, Substantially Equivalent on 2020-07-27. Applicant: Tribofilm Research, Inc.. Device class: 2.
Clearance details
- Applicant
- Tribofilm Research, 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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More clearances from Tribofilm Research, Inc.
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