ASPIRE Cristalle
FDA 510(k) K173132 · Fujifilm Medical Systems U.S.A, Inc.
510(k) numberK173132
Submission
- Device name
- ASPIRE Cristalle
- Applicant
- Fujifilm Medical Systems U.S.A, Inc.
Stamford, CT, US - Received
- September 29, 2017
- Decision date
- October 27, 2017
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
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Questions and answers
When was ASPIRE Cristalle cleared by the FDA?
ASPIRE Cristalle (K173132) received a 510(k) decision of Substantially Equivalent on October 27, 2017, 28 days after the submission was received.
What is the product code of K173132?
The FDA product code is MUE – Full Field Digital, System, X-Ray, Mammographic, a Class II (moderate risk) device regulated under 21 CFR 892.1715.