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MRCP+ version 2 (MRCP+ v2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233930
510(k) Type
Traditional
Applicant
Perspectum
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/13/2024
Days to Decision
90 days
Submission Type
Summary

MRCP+ version 2 (MRCP+ v2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233930
510(k) Type
Traditional
Applicant
Perspectum
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/13/2024
Days to Decision
90 days
Submission Type
Summary