AccuMeasure System— 510(k) DEN210032
UnknownRQMIS, Inc.
FDA 510(k) clearance DEN210032 for AccuMeasure System, Unknown on 2022-07-26. Applicant: RQMIS, Inc.. Device class: 2.
Clearance details
- Applicant
- RQMIS, Inc.
- Product code
- Code QTH
- Device class
- Class 2
- Regulation
- 21 CFR 876.1530
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Amesbury, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.