Parallel— 510(k) DEN200029
UnknownMahana Therapeutics, Inc.
FDA 510(k) clearance DEN200029 for Parallel, Unknown on 2020-11-25. Applicant: Mahana Therapeutics, Inc.. Device class: 2.
Clearance details
- Applicant
- Mahana Therapeutics, Inc.
- Product code
- Code QMY
- Device class
- Class 2
- Regulation
- 21 CFR 876.5960
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- San Francisco, CA, US
Recent devices under product code QMY
view allData sourced from openFDA. This site is unofficial and independent of the FDA.