BAROnova Access Sheath Kit— 510(k) K191078
UnknownBaronova, Inc.
FDA 510(k) clearance K191078 for BAROnova Access Sheath Kit, Unknown on 2019-07-22. Applicant: Baronova, Inc.. Device class: 2.
Clearance details
- Applicant
- Baronova, Inc.
- Product code
- Code QGG
- Device class
- Class 2
- Regulation
- 21 CFR 876.1510
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- San Carlos, CA, US
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