BAROnova Access Sheath Kit— 510(k) K191078

Unknown

Baronova, Inc.

FDA 510(k) clearance K191078 for BAROnova Access Sheath Kit, Unknown on 2019-07-22. Applicant: Baronova, Inc..

Clearance details

Applicant: Baronova, Inc.
Product code: Code QGG
Advisory panel: Gastroenterology, Urology
Date received: 2019-04-23
Decision date: 2019-07-22
Decision: Unknown
Clearance type: Traditional
Location: San Carlos, CA, US

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