First Relief v1— 510(k) K202940
Substantially EquivalentDyansys, Inc.
FDA 510(k) clearance K202940 for First Relief v1, Substantially Equivalent on 2020-12-29. Applicant: Dyansys, Inc.. Device class: 2.
Clearance details
- Applicant
- Dyansys, Inc.
- Product code
- Code QHH
- Device class
- Class 2
- Regulation
- 21 CFR 876.5340
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Mateo, CA, US
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