cmTriage— 510(k) K183285
Substantially EquivalentCuremetrix, Inc.
FDA 510(k) clearance K183285 for cmTriage, Substantially Equivalent on 2019-03-08. Applicant: Curemetrix, Inc.. Device class: 2.
Clearance details
- Applicant
- Curemetrix, Inc.
- Product code
- Code QFM
- Device class
- Class 2
- Regulation
- 21 CFR 892.2080
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- La Jolla, CA, US
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