ManaFlow— 510(k) K200353
Substantially EquivalentManamed, Inc.
FDA 510(k) clearance K200353 for ManaFlow, Substantially Equivalent on 2020-08-06. Applicant: Manamed, Inc.. Device class: 2.
Clearance details
- Applicant
- Manamed, Inc.
- Product code
- Code JOW
- Device class
- Class 2
- Regulation
- 21 CFR 870.5800
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Las Vegas, NV, US
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